A Novel Homozygous Mutation in CYP11A1 Gene is Associated with Severe Adrenal Insufficiency in 46, XX Patient-Reference-Cited by-同舟云学术

A Novel Homozygous Mutation in CYP11A1 Gene is Associated with Severe Adrenal Insufficiency in 46, XX Patient

Author:

Kara Ozlem¹^ORCID,Gorukmez Orhan²^ORCID,Ekici Arzu³^ORCID,Celik Fatih⁴^ORCID

Affiliation:

1. Pediatric Endocrinology, University of Health Sciences Bursa, Yuksek Ihtisas Training and Research Hospital, Bursa, Turkey

2. Genetics, University of Health Sciences Bursa, Yuksek Ihtisas Training and Research Hospital, Bursa, Turkey

3. Pediatric Neurology, University of Health Sciences Bursa, Yuksek Ihtisas Training and Research Hospital, Bursa, Turkey

4. Pediatric Surgical, Bursa Uludag University Medical School, Bursa, Turkey

Publisher

Informa UK Limited

Subject

General Medicine,Pathology and Forensic Medicine,Pediatrics, Perinatology, and Child Health

Link

Reference9 articles.

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