LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss (2019)
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
Parent Publication: European Journal of Medical Genetics
Issue: 12
ISSN: 1769-7212