P450C17 (CYP17) Deficiency in Native Mexican Patient with a Novel CYP17A1 Mutation-Reference-Cited by-同舟云学术

P450C17 (CYP17) Deficiency in Native Mexican Patient with a Novel CYP17A1 Mutation

Published:2011-01 Issue:1 Volume:17 Page:99-103
ISSN:1530-891X
Container-title:Endocrine Practice
language:en
Short-container-title:Endocrine Practice

Author:

Durán Pérez Edgar G.,del Rincón Lourdes González,Moreno Loza Oscar T.,Martín de Saro Monica D.,Palomo Antonio Segovia,Pedraza Valentín Sánchez,Alfaro Susana Kofman,Queipo García Gloria E.

Publisher

Elsevier BV

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

Link

http://aace.metapress.com/index/P64001441558243V.pdf

Reference14 articles.

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2. P450c17 deficiency: Clinical and molecular characterization of six patients;Rosa;J Clin Endocrinol Metab,2007

3. The role of adrenal steroidogenesis in arterial hypertension;Mohaupt;Endocr Rev,2008

4. Disorders of sex development;Achermann,2008

5. Male pseudohermaphroditism due to 17 alphahydroxylase deficiency.;New;J Clin Invest.,1970

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2. New Genetic Abnormalities in Non-21a-Hydroxylase-Deficiency Congenital Adrenal Hyperplasia;Sexual Development;2013

3. Primary amenorrhea in two sisters: description of a Mexican family with 17α hydroxylase-17 lyase deficiency caused by arginine – stop mutation;Gynecological Endocrinology;2012-02-06