A mutation update for the <i>FLNC</i> gene in myopathies and cardiomyopathies
Job A.J. Verdonschot(Maastricht University Medical Centre), Han G. Brunner(Radboud University Nijmegen)
Cited by 178
Related Papers
Abnormal Behavior Associated with a Point Mutation in the Structural Gene for Monoamine Oxidase A
|Science|1993|1.6k
Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1
|Nature Genetics|2008|818