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LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss. (2019)

First Author: Al-Amri AH

Attributed to: Identification of Major Risk Alleles for Schizophrenia in Consanguineous Families funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ejmg.2018.11.026

PubMed Identifier: 30476627

Publication URI: http://europepmc.org/abstract/MED/30476627

Type: Journal Article/Review

Volume: 62

Parent Publication: European journal of medical genetics

Issue: 12

ISSN: 1769-7212