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

First Author: Feichtinger RG
Attributed to:  Mitochondrial Genetics funded by MRC


No abstract provided

Bibliographic Information

Digital Object Identifier:

PubMed Identifier: 28942965

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Type: Journal Article/Review

Volume: 101

Parent Publication: American journal of human genetics

Issue: 4

ISSN: 0002-9297