A new missense mutation, Arg719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy

M. W. Consevage, G. C. Salada, B. G. Baylen, Roger Ladda, P. K. Rogan

Research output: Contribution to journalComment/debate

11 Citations (Scopus)
Original languageEnglish (US)
Number of pages1
JournalHuman Molecular Genetics
Volume3
Issue number9
DOIs
StatePublished - Sep 1 1994

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Familial Hypertrophic Cardiomyopathy
Myosin Heavy Chains
Missense Mutation
Genes

All Science Journal Classification (ASJC) codes

  • Molecular Biology
  • Genetics
  • Genetics(clinical)

Cite this

Consevage, M. W. ; Salada, G. C. ; Baylen, B. G. ; Ladda, Roger ; Rogan, P. K. / A new missense mutation, Arg719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy. In: Human Molecular Genetics. 1994 ; Vol. 3, No. 9.
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A new missense mutation, Arg719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy. / Consevage, M. W.; Salada, G. C.; Baylen, B. G.; Ladda, Roger; Rogan, P. K.

In: Human Molecular Genetics, Vol. 3, No. 9, 01.09.1994.

Research output: Contribution to journalComment/debate

TY - JOUR

T1 - A new missense mutation, Arg719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy

AU - Consevage, M. W.

AU - Salada, G. C.

AU - Baylen, B. G.

AU - Ladda, Roger

AU - Rogan, P. K.

PY - 1994/9/1

Y1 - 1994/9/1

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U2 - 10.1093/hmg/3.9.1716

DO - 10.1093/hmg/3.9.1716

M3 - Comment/debate

AN - SCOPUS:0007055077

VL - 3

JO - Human Molecular Genetics

JF - Human Molecular Genetics

SN - 0964-6906

IS - 9

ER -