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Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies. (2017)

First Author: Feichtinger RG

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/10.1016/j.ajhg.2017.08.015

PubMed Identifier: 28942965

Publication URI: http://europepmc.org/abstract/MED/28942965

Type: Journal Article/Review

Volume: 101

Parent Publication: American journal of human genetics

Issue: 4

ISSN: 0002-9297