Steroid 21‐hydroxylase gene mutational spectrum in 454 Argentinean patients: genotype–phenotype correlation in a large cohort of patients with congenital adrenal hyperplasia-Reference-Cited by-同舟云学术

Steroid 21‐hydroxylase gene mutational spectrum in 454 Argentinean patients: genotype–phenotype correlation in a large cohort of patients with congenital adrenal hyperplasia

Published:2011-09-07 Issue:4 Volume:75 Page:427-435
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:Clinical Endocrinology

Author:

Marino Roxana¹,Ramirez Pablo¹,Galeano Jesica¹,Perez Garrido Natalia¹,Rocco Carlos²,Ciaccio Marta¹,Warman Diana M.¹,Guercio Gabriela¹,Chaler Eduardo¹,Maceiras Mercedes¹,Bergadá Ignacio³,Gryngarten Mirta³,Balbi Viviana⁴,Pardes Esther⁵,Rivarola Marco A.¹,Belgorosky Alicia¹

Affiliation:

1. Endocrinology Service, Hospital de Pediatria Garrahan, Buenos Aires

2. Laboratory of Cellular Biology and Retrovirus, Hospital de Pediatria Garrahan

3. Endocrinology Service, Hospital de Niños Gutierrez, Buenos Aires

4. Endocrinology Service, Hospital de Niños SSM Ludovica, La Plata

5. Endocrinology Service, Hospital JM Ramos Mejía, Buenos Aires, Argentina

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1365-2265.2011.04123.x