Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies (2017)
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/10.17863/cam.13698
Publication URI: https://www.repository.cam.ac.uk/handle/1810/267768
Type: Journal Article/Review