Five New Cases of 46,XX Aromatase Deficiency: Clinical Follow-Up From Birth to Puberty, a Novel Mutation, and a Founder Effect-Reference-Cited by-同舟云学术

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Five New Cases of 46,XX Aromatase Deficiency: Clinical Follow-Up From Birth to Puberty, a Novel Mutation, and a Founder Effect

Published:2015-02 Issue:2 Volume:100 Page:E301-E307
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

Marino Roxana,Perez Garrido Natalia,Costanzo Mariana,Guercio Gabriela,Juanes Matías,Rocco Carlos,Ramirez Pablo,Warman Diana M.,Ciaccio Marta,Pena Gladys,Feyling José García,Miras Mirta,Rivarola Marco A.,Belgorosky Alicia,Saraco Nora

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Cited by 34 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Structures and functions of human placental aromatase and steroid sulfatase, two key enzymes in estrogen biosynthesis;Steroids;2023-08

2. 46,XX aromatase deficiency: A single-center experience with the varied spectrum and recurrent variants, and a systematic review of hormonal parameters;Annales d'Endocrinologie;2023-06

3. Aromatase in human physiology and pathology: implications of human aromatase deficiency;Genetic Steroid Disorders;2023

4. Congenital disorders of estrogen biosynthesis and action;Best Practice & Research Clinical Endocrinology & Metabolism;2021-09

5. Sex determination, gonadal sex differentiation, and plasticity in vertebrate species;Physiological Reviews;2021-07-01

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