Inactivation of PKHD1 results in a liver phenotype characteristic of autosomal recessive polycystic kidney disease (ARPKD)
Rachel Gallagher Ernie Esquivel; Xin Tian; Tiffany Samaroo; Dhanpat Jain; Luiz Onuchie; Lisa Guay Woodford; Gregory Germino; Stefan Somlo; Abstracts issue journal of the american Society of Nephrology - JASN 2004 St. Louis
Journal of the American Society of Nephrology Baltimore v. 15, Abstracts issue, p. 56A res. SU-FC061, 2004Baltimore 2004
Localização: FM - Fac. Medicina (BCSEP 236 2004 ) e outros locais(Acessar)
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bcsep 236 2010
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