Mutations in the gamma2 subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis
Year: 2001
Type: article
Source: Human Molecular Genetics
Author: E. Blair
Institutions: Centre for Human Genetics, University of Oxford
Language: English
Subfield: Cardiology and Cardiovascular Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W2107724201
