Format

Send to:

Choose Destination
See comment in PubMed Commons below
J Med Genet. 2001 Dec;38(12):E43.

Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations.

PMID:
11748309
[PubMed - indexed for MEDLINE]
PMCID:
PMC1734772
Free PMC Article
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for HighWire Icon for PubMed Central
    Loading ...
    Write to the Help Desk