17-hydroxylase/17,20-lyase deficiency due to a R96Q mutation causing hypertension and poor breast development
Deeb, Asma ; Al Suwaidi, Hana ; Attia, Salima ; Al Ameri, Ahlam
Endocrinology, diabetes & metabolism case reports, 2015-11, Vol.2015, p.150069-150069 [Periódico revisado por pares]England: Bioscientifica Ltd
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