reference/3298884

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/3298884

Outgoing Links

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publicationName	Journal of Human Genetics
startingPage	1099
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bibliographicCitation	Liaqat K, Chiu I, Lee K, Chakchouk I, Andrade-Elizondo PB, Santos-Cortez RLP, Hussain S, Nawaz S, Ansar M, Khan MN, Basit S, Schrauwen I, Ahmad W, Leal SM. Novel missense and 3′-UTR splice site variants in LHFPL5 cause autosomal recessive nonsyndromic hearing impairment. Journal of Human Genetics. 2018 Sep 03;63(11):1099–107. doi: 10.1038/s10038-018-0502-3.
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date	2018-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC6202120 https://doi.org/10.1038/s10038-018-0502-3 https://pubmed.ncbi.nlm.nih.gov/30177809
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language	English
source	https://scigraph.springernature.com/ https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Novel missense and 3′-UTR splice site variants in LHFPL5 cause autosomal recessive nonsyndromic hearing impairment
discusses	http://id.nlm.nih.gov/mesh/M0505024 http://id.nlm.nih.gov/mesh/M0359363 http://id.nlm.nih.gov/mesh/M0030068 http://id.nlm.nih.gov/mesh/M0013341
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Incoming Links

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Total number of triples: 51.