reference/5972681

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/5972681

Outgoing Links

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bibliographicCitation	Santos-Cortez RL, Faridi R, Rehman AU, Lee K, Ansar M, Wang X, Morell RJ, Isaacson R, Belyantseva IA, Dai H, Acharya A, Qaiser TA, Muhammad D, Ali RA, Shams S, Hassan MJ, Shahzad S, Raza SI, Bashir ZE, Smith JD, Nickerson DA, Bamshad MJ; University of Washington Center for Mendelian Genomics, Riazuddin S, Ahmad W, Friedman TB, Leal SM. Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2. Am J Hum Genet. 2016 Feb 04;98(2):331–8. PMID: 26805784; PMCID: PMC4746333.
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date	2016-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC4746333 https://pubmed.ncbi.nlm.nih.gov/26805784 https://doi.org/10.1016/j.ajhg.2015.12.004
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2
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Total number of triples: 99.