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
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author Sahana M Srinivas
Sowjanya G Thimmaiah
Radha Venkatesan
Raghupathy Palany
author_facet Sahana M Srinivas
Sowjanya G Thimmaiah
Radha Venkatesan
Raghupathy Palany
author_sort Sahana M Srinivas
collection DOAJ
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issn 2319-7250
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publisher Wolters Kluwer Medknow Publications
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spelling doaj.art-2299def737c54ef897f4c0f814df9aa42022-12-21T17:49:49ZengWolters Kluwer Medknow PublicationsIndian Journal of Paediatric Dermatology2319-72502020-01-0121435435510.4103/ijpd.IJPD_58_20H syndrome: A rare case with homozygous mutation in SLC29A3 geneSahana M SrinivasSowjanya G ThimmaiahRadha VenkatesanRaghupathy Palanyhttp://www.ijpd.in/article.asp?issn=2319-7250;year=2020;volume=21;issue=4;spage=354;epage=355;aulast=Srinivas
spellingShingle Sahana M Srinivas
Sowjanya G Thimmaiah
Radha Venkatesan
Raghupathy Palany
H syndrome: A rare case with homozygous mutation in SLC29A3 gene
Indian Journal of Paediatric Dermatology
title H syndrome: A rare case with homozygous mutation in SLC29A3 gene
title_full H syndrome: A rare case with homozygous mutation in SLC29A3 gene
title_fullStr H syndrome: A rare case with homozygous mutation in SLC29A3 gene
title_full_unstemmed H syndrome: A rare case with homozygous mutation in SLC29A3 gene
title_short H syndrome: A rare case with homozygous mutation in SLC29A3 gene
title_sort h syndrome a rare case with homozygous mutation in slc29a3 gene
url http://www.ijpd.in/article.asp?issn=2319-7250;year=2020;volume=21;issue=4;spage=354;epage=355;aulast=Srinivas
work_keys_str_mv AT sahanamsrinivas hsyndromeararecasewithhomozygousmutationinslc29a3gene
AT sowjanyagthimmaiah hsyndromeararecasewithhomozygousmutationinslc29a3gene
AT radhavenkatesan hsyndromeararecasewithhomozygousmutationinslc29a3gene
AT raghupathypalany hsyndromeararecasewithhomozygousmutationinslc29a3gene