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

Michael W. Consevage, Grant C. Salada, Barry G. Baylen, Roger L. Ladda, Peter K. Rogan

Research output: Contribution to journalComment/debate

41 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)1025-1026
Number of pages2
JournalHuman molecular genetics
Volume3
Issue number6
DOIs
StatePublished - Jun 1 1994

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Molecular Sequence Data
Familial Hypertrophic Cardiomyopathy
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 11
DNA Primers
Myosin Heavy Chains
Chromosome Mapping
Chromosomes, Human, Pair 1
Hypertrophic Cardiomyopathy
Missense Mutation
Pedigree
Myosins
Glutamine
Point Mutation
Arginine
Amino Acid Sequence
Myocardium
Reference Values
Polymerase Chain Reaction

All Science Journal Classification (ASJC) codes

  • Molecular Biology
  • Genetics
  • Genetics(clinical)

Cite this

Consevage, Michael W. ; Salada, Grant C. ; Baylen, Barry G. ; Ladda, Roger L. ; Rogan, Peter 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. 6. pp. 1025-1026.
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A new missense mutation, Arg719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy. / Consevage, Michael W.; Salada, Grant C.; Baylen, Barry G.; Ladda, Roger L.; Rogan, Peter K.

In: Human molecular genetics, Vol. 3, No. 6, 01.06.1994, p. 1025-1026.

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, Michael W.

AU - Salada, Grant C.

AU - Baylen, Barry G.

AU - Ladda, Roger L.

AU - Rogan, Peter K.

PY - 1994/6/1

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U2 - 10.1093/hmg/3.6.1025

DO - 10.1093/hmg/3.6.1025

M3 - Comment/debate

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VL - 3

SP - 1025

EP - 1026

JO - Human Molecular Genetics

JF - Human Molecular Genetics

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