A R644C mutation within lamin A extends the mutations causing dilated cardiomyopathy.

Human mutation

Volumn 17, Issue 2, 2001, Pages 154-

  Genschel, J ^a   Bochow, B ^a   Kuepferling, S ^a   Ewert, R ^a   Hetzer, R ^a   Lochs, H ^a   Schmidt, H ^a  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; LAMIN; LAMIN A; NUCLEAR PROTEIN;

AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; CHEMISTRY; CONGESTIVE CARDIOMYOPATHY; GENETICS; HUMAN; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PATHOLOGY;

AMINO ACID SUBSTITUTION; CARDIOMYOPATHY, DILATED; DNA; DNA MUTATIONAL ANALYSIS; HUMANS; LAMIN TYPE A; LAMINS; MUTATION, MISSENSE; NUCLEAR PROTEINS;

EID: 0035256432     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/1098-1004(200102)17:2<154::aid-humu11>3.0.co;2-r     Document Type: Article

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