Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 gene [5]

Clinical Genetics

Volumn 56, Issue 3, 1999, Pages 244-246

  Andersen, P S ^a   Havndrup, O ^a   Bundgaard, H ^a   Larsen, L A ^a   Vuust, J ^a   Kjeldsen, K ^a   Christiansen, M ^a  

^a STATENS SERUM INSTITUT   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; CYSTEINE; MYOSIN HEAVY CHAIN;

AGED; CASE REPORT; CODON; EXON; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; LETTER; MALE; MISSENSE MUTATION; ONSET AGE; PRIORITY JOURNAL;

AGE OF ONSET; AGED; CARDIOMYOPATHY, HYPERTROPHIC; FEMALE; HUMANS; MALE; MUTATION, MISSENSE; MYOSIN HEAVY CHAINS; PEDIGREE;

EID: 0032723888     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.1999.560313.x     Document Type: Letter

References (9)