Corrigendum: A new missense mutation, Arg719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy (Human Molecular Genetics (1994) 3 (1025-1026))

M. W. Consevage; G. C. Salada; B. G. Baylen; R. L. Ladda; P. K. Rogan

Corrigendum: A new missense mutation, Arg719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy (Human Molecular Genetics (1994) 3 (1025-1026))

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

Department of Pediatrics

Research output: Contribution to journal › Comment/debate › peer-review

Original language	English (US)
Number of pages	1
Journal	Human molecular genetics
Volume	3
Issue number	9
State	Published - Jan 1 1994

All Science Journal Classification (ASJC) codes

Molecular Biology
Genetics
Genetics(clinical)

Cite this

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title = "Corrigendum: A new missense mutation, Arg719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy (Human Molecular Genetics (1994) 3 (1025-1026))",

author = "Consevage, {M. W.} and Salada, {G. C.} and Baylen, {B. G.} and Ladda, {R. L.} and Rogan, {P. K.}",

year = "1994",

month = jan,

day = "1",

language = "English (US)",

volume = "3",

journal = "Human molecular genetics",

issn = "0964-6906",

publisher = "Oxford University Press",

number = "9",

}

Corrigendum: A new missense mutation, Arg719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy (Human Molecular Genetics (1994) 3 (1025-1026)). / Consevage, M. W.; Salada, G. C.; Baylen, B. G. et al.
In: Human molecular genetics, Vol. 3, No. 9, 01.01.1994.

Research output: Contribution to journal › Comment/debate › peer-review

TY - JOUR

T1 - Corrigendum

T2 - A new missense mutation, Arg719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy (Human Molecular Genetics (1994) 3 (1025-1026))

AU - Consevage, M. W.

AU - Salada, G. C.

AU - Baylen, B. G.

AU - Ladda, R. L.

AU - Rogan, P. K.

PY - 1994/1/1

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UR - http://www.scopus.com/inward/citedby.url?scp=0027968268&partnerID=8YFLogxK

M3 - Comment/debate

AN - SCOPUS:0027968268

SN - 0964-6906

VL - 3

JO - Human molecular genetics

JF - Human molecular genetics

IS - 9

ER -

Corrigendum: A new missense mutation, Arg719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy (Human Molecular Genetics (1994) 3 (1025-1026))

All Science Journal Classification (ASJC) codes

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