RGD Reference Report - Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations. - Rat Genome Database

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

Authors: Andersen, PS  Havndrup, O  Bundgaard, H  Moolman-Smook, JC  Larsen, LA  Mogensen, J  Brink, PA  Borglum, AD  Corfield, VA  Kjeldsen, K  Vuust, J  Christiansen, M 
Citation: Andersen PS, etal., J Med Genet. 2001 Dec;38(12):E43.
RGD ID: 1580241
Pubmed: PMID:11748309   (View Abstract at PubMed)
PMCID: PMC1734772   (View Article at PubMed Central)

Abstract for this paper unavailable



RGD Manual Disease Annotations    Click to see Annotation Detail View
Object SymbolSpeciesTermQualifierEvidenceWithNotesSourceOriginal Reference(s)
MYL2Humanfamilial hypertrophic cardiomyopathy  IAGP DNA:missense mutations more ...RGD 
Myl2Mousefamilial hypertrophic cardiomyopathy  ISOMYL2 (Homo sapiens)DNA:missense mutations more ...RGD 
Myl2Ratfamilial hypertrophic cardiomyopathy  ISOMYL2 (Homo sapiens)DNA:missense mutations more ...RGD 

Objects Annotated

Genes (Rattus norvegicus)
Myl2  (myosin light chain 2)

Genes (Mus musculus)
Myl2  (myosin, light polypeptide 2, regulatory, cardiac, slow)

Genes (Homo sapiens)
MYL2  (myosin light chain 2)

Objects referenced in this article
Gene MYL11 myosin light chain 11 Homo sapiens
Gene MYL3 myosin light chain 3 Homo sapiens
Gene Myl3 myosin, light polypeptide 3 Mus musculus
Gene Mylpf myosin light chain, phosphorylatable, fast skeletal muscle Mus musculus
Gene Myl11 myosin light chain 11 Rattus norvegicus
Gene Myl3 myosin light chain 3 Rattus norvegicus

Additional Information