Mutations of Presenilin Genes in Dilated Cardiomyopathy and Heart Failure
Duanxiang Li(University of Miami), Ray E. Hershberger(University of Miami), Jessica D. Kushner(Oregon Health & Science University), Petra Jakobs(Oregon Health & Science University), M. Litt(Hospital of the University of Pennsylvania), Sharie B. Parks(Oregon Health & Science University), Julie Partain(Oregon Health & Science University), Randal R. Nixon(Oregon Health & Science University), Robert P. Irwin(Oregon Health & Science University), Deirdre Nauman(Oregon Health & Science University), Charles N. Allen(Oregon Health & Science University), Donna R. Burgess(Oregon Health & Science University), Susan Ludwigsen(Fox Chase Cancer Center)
Cited by 183
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