H syndrome: A rare case with homozygous mutation in SLC29A3 gene
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2020-01-01
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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 |
first_indexed | 2024-12-23T10:54:07Z |
format | Article |
id | doaj.art-2299def737c54ef897f4c0f814df9aa4 |
institution | Directory Open Access Journal |
issn | 2319-7250 |
language | English |
last_indexed | 2024-12-23T10:54:07Z |
publishDate | 2020-01-01 |
publisher | Wolters Kluwer Medknow Publications |
record_format | Article |
series | Indian Journal of Paediatric Dermatology |
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 |