reference/12851158

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/12851158

Outgoing Links

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contentType	Journal Article
endingPage	101
issn	0914-3505 1741-4520
issueIdentifier	3
pageRange	99-101
publicationName	Congenital Anomalies
startingPage	99
hasFundingAgency	http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_53c0aa3977ca6c88b95b019bc3aefbb2 http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_e0b47dc2503df2a41574fa5843ecd0cd
bibliographicCitation	Al-Zahrani HS, Al-Tala S, Mohamoud HSA, Al-Shehri BA, Al-Fadhel S, Al-Qurashi A, Al-Bishri A, Al-Aama JY, Kang C, Betz RC, Jelani M. Novel compound heterozygous and homozygous variants of laminin subunit β3 gene underlie non-Herlitz junctional epidermolysis bullosa in two paternal half-brothers from Saudi Arabia. Congenit Anom (Kyoto). 2019 May;59(3):99–101. doi: 10.1111/cga.12294. PMID: 29900604.
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date	2018-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1111/cga.12294 https://pubmed.ncbi.nlm.nih.gov/29900604
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/29811 https://portal.issn.org/resource/ISSN/0914-3505 https://portal.issn.org/resource/ISSN/1741-4520
language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Novel compound heterozygous and homozygous variants of laminin subunit β3 gene underlie non‐Herlitz junctional epidermolysis bullosa in two paternal half‐brothers from Saudi Arabia
discusses	http://id.nlm.nih.gov/mesh/M0024220
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Incoming Links

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isDiscussedBy	http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID3914

Total number of triples: 54.