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1
Correction: Association of SMAD4 mutation with patient demographics, tumor characteristics, and clinical outcomes in colorectal cancer
Material Type:
Artigo
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Correction: Association of SMAD4 mutation with patient demographics, tumor characteristics, and clinical outcomes in colorectal cancer

PloS one, 2017-05, Vol.12 (5), p.e0178275-e0178275 [Periódico revisado por pares]

United States: Public Library of Science

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2
Correction: A Novel Quantitative Hemolytic Assay Coupled with Restriction Fragment Length Polymorphisms Analysis Enabled Early Diagnosis of Atypical Hemolytic Uremic Syndrome and Identified Unique Predisposing Mutations in Japan
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Artigo
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Correction: A Novel Quantitative Hemolytic Assay Coupled with Restriction Fragment Length Polymorphisms Analysis Enabled Early Diagnosis of Atypical Hemolytic Uremic Syndrome and Identified Unique Predisposing Mutations in Japan

Yoshida, Yoko ; Miyata, Toshiyuki ; Matsumoto, Masanori ; Shirotani-Ikejima, Hiroko ; Uchida, Yumiko ; Ohyama, Yoshifumi ; Kokubo, Tetsuro ; Fujimura, Yoshihiro

PloS one, 2017-05, Vol.12 (5), p.e0178015-e0178015 [Periódico revisado por pares]

United States: Public Library of Science

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3
Correction: A Novel GJA8 Mutation (p.V44A) Causing Autosomal Dominant Congenital Cataract
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Artigo
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Correction: A Novel GJA8 Mutation (p.V44A) Causing Autosomal Dominant Congenital Cataract

Zhu, Yanan ; Yu, Hao ; Wang, Wei ; Gong, Xiaohua ; Yao, Ke

PloS one, 2015-05, Vol.10 (5), p.e0125949-e0125949 [Periódico revisado por pares]

United States: Public Library of Science

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4
Correction: Species-Specific Codon Context Rules Unveil Non-Neutrality Effects of Synonymous Mutations
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Artigo
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Correction: Species-Specific Codon Context Rules Unveil Non-Neutrality Effects of Synonymous Mutations

Moura, Gabriela R ; Pinheiro, Miguel ; Freitas, Adelaide ; Oliveira, José L ; Frommlet, Jörg C ; Carreto, Laura ; Soares, Ana R ; Bezerra, Ana R ; Santos, Manuel A S

PloS one, 2015-12, Vol.10 (12), p.e0145593-e0145593 [Periódico revisado por pares]

United States: Public Library of Science

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5
Correction: Novel Compound Heterozygous Mutations in MYO7A Associated with Usher Syndrome 1 in a Chinese Family
Material Type:
Artigo
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Correction: Novel Compound Heterozygous Mutations in MYO7A Associated with Usher Syndrome 1 in a Chinese Family

Gao, Xue ; Wang, Guo-Jian ; Yuan, Yong-Yi ; Xin, Feng ; Han, Ming-Yu ; Lu, Jing-Qiao ; Zhao, Hui ; Yu, Fei ; Xu, Jin-Cao ; Zhang, Mei-Guang ; Dong, Jiang ; Lin, Xi ; Dai, Pu

PloS one, 2015-10, Vol.10 (10), p.e0137883-e0137883 [Periódico revisado por pares]

United States: Public Library of Science

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6
Large, three-generation human families reveal post-zygotic mosaicism and variability in germline mutation accumulation
Material Type:
Artigo
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Large, three-generation human families reveal post-zygotic mosaicism and variability in germline mutation accumulation

Sasani, Thomas A ; Pedersen, Brent S ; Gao, Ziyue ; Baird, Lisa ; Przeworski, Molly ; Jorde, Lynn B ; Quinlan, Aaron R

eLife, 2019-09, Vol.8 [Periódico revisado por pares]

England: eLife Sciences Publications Ltd

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7
Genome-wide DNA mutations in Arabidopsis plants after multigenerational exposure to high temperatures
Material Type:
Artigo
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Genome-wide DNA mutations in Arabidopsis plants after multigenerational exposure to high temperatures

Lu, Zhaogeng ; Cui, Jiawen ; Wang, Li ; Teng, Nianjun ; Zhang, Shoudong ; Lam, Hon-Ming ; Zhu, Yingfang ; Xiao, Siwei ; Ke, Wensi ; Lin, Jinxing ; Xu, Chenwu ; Jin, Biao

Genome Biology, 2021-05, Vol.22 (1), p.160-160, Article 160 [Periódico revisado por pares]

England: BioMed Central Ltd

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8
Correction: Mutation rules and the evolution of sparseness and modularity in biological systems
Material Type:
Artigo
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Correction: Mutation rules and the evolution of sparseness and modularity in biological systems

PloS one, 2015-03, Vol.10 (3), p.e0118129-e0118129 [Periódico revisado por pares]

United States: Public Library of Science

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9
Correction: Clinical significance of cerebral microbleeds locations in CADASIL with R544C NOTCH3 mutation
Material Type:
Artigo
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Correction: Clinical significance of cerebral microbleeds locations in CADASIL with R544C NOTCH3 mutation

Lee, Jung Seok ; Kang, Chul-hoo ; Park, Sukh Que ; Choi, H Alex ; Sim, Ki-Bum

PloS one, 2015-04, Vol.10 (4), p.e0125297-e0125297 [Periódico revisado por pares]

United States: Public Library of Science

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10
Correction: PDCD10 gene mutations in multiple cerebral cavernous malformations
Material Type:
Artigo
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Correction: PDCD10 gene mutations in multiple cerebral cavernous malformations

PloS one, 2015-04, Vol.10 (4), p.e0123486-e0123486 [Periódico revisado por pares]

United States: Public Library of Science

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