Coding Sequence Mutations Identified in <i>MYH7, TNNT2, SCN5A, CSRP3, LBD3</i>, and <i>TCAP</i> from 313 Patients with Familial or Idiopathic Dilated Cardiomyopathy
Ray E. Hershberger(University of Miami), M. Litt(Hospital of the University of Pennsylvania), Jessica D. Kushner(Oregon Health & Science University), Petra Jakobs(Oregon Health & Science University), Sharie B. Parks(Oregon Health & Science University), Duanxiang Li(University of Miami), Julie Partain(Oregon Health & Science University), Deirdre Nauman(Oregon Health & Science University), Donna R. Burgess(Oregon Health & Science University), Susan Ludwigsen(Fox Chase Cancer Center)
Cited by 194
Related Papers
Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1
|Nature Genetics|1994|776
A Comprehensive Human Linkage Map with Centimorgan Density
|Science|1994|537
Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA
|Human Molecular Genetics|1998|447
The human dopamine D2 receptor gene is located on chromosome 11 at q22-q23 and identifies a TaqI RFLP.
|PubMed|1989|424
SECONDARY STRUCTURE IN RIBONUCLEIC ACIDS
|Proceedings of the National Academy of Sciences|1959|363