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Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family (2018)

First Author: Kullar P

Attributed to: Investigation of the function of the ER/mitochondria contact sites in cell physiology and disease funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/brain/awx295

PubMed Identifier: 29182774

Publication URI: http://europepmc.org/abstract/MED/29182774

Type: Journal Article/Review

Parent Publication: Brain

Issue: 1