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The spectrum of CYP21A2 gene mutations from 16 families of congenital adrenal hyperplasia: Genotype-phenotype correlation
Author(s) -
Subbiah Sridhar,
Ramajayam Govindhan,
Balasankar Soundian,
Maheshkumar Poomarimuthu,
Karuppasamy Nallan,
SanthanakrishnanRamesh kumar,
Subbiah Eagappan,
Vasanthiy Natarajan,
Srinivasan Jayaraman
Publication year - 2021
Publication title -
indian journal of endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.456
H-Index - 28
eISSN - 2230-9500
pISSN - 2230-8210
DOI - 10.4103/ijem.ijem_442_21
Subject(s) - congenital adrenal hyperplasia , 21 hydroxylase , genetics , genotype , gene , intron , mutation , population , gene mutation , restriction fragment length polymorphism , medicine , microbiology and biotechnology , biology , environmental health

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