H syndrome: A rare case with homozygous mutation in SLC29A3 gene

H syndrome: A rare case with homozygous mutation in SLC29A3 gene

Bibliographic Details
Main Authors: Sahana M Srinivas, Sowjanya G Thimmaiah, Radha Venkatesan, Raghupathy Palany
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2020-01-01
Series:Indian Journal of Paediatric Dermatology
Online Access:http://www.ijpd.in/article.asp?issn=2319-7250;year=2020;volume=21;issue=4;spage=354;epage=355;aulast=Srinivas
Description
ISSN:2319-7250

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