Literature DB >> 26388637

CYP21A2 gene mutation in South Indian children with congenital adrenal hyperplasia.

Ramaswamy Ganesh1, Natarajan Suresh, Lalitha Janakiraman, Karnam Ravikumar.   

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Year:  2015        PMID： 26388637

Source DB:  PubMed          Journal:  Indian Pediatr        ISSN： 0019-6061            Impact factor:   1.411


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  1 in total

1.  Clinical application of a novel next generation sequencing assay for CYP21A2 gene in 310 cases of 21- hydroxylase congenital adrenal hyperplasia from India.

Authors:  Priyanka Gangodkar; Vaman Khadilkar; P Raghupathy; Rakesh Kumar; Archana Arya Dayal; Devi Dayal; Ahila Ayyavoo; Tushar Godbole; Rahul Jahagirdar; Kavitha Bhat; Neerja Gupta; Sadishkumar Kamalanathan; Sujatha Jagadeesh; Shatakshi Ranade; Nikhil Lohiya; Rashmi Lote Oke; Karthik Ganesan; Kavita Khatod; Meenal Agarwal; Nikhil Phadke; Anuradha Khadilkar
Journal:  Endocrine       Date:  2020-09-18       Impact factor: 3.633
  1 in total

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