An ARG403GLN β-myosin heavy chain gene mutation identified in an Italian family with hypertrophic cardiomyopathy: Description of clinical features of the family members [2]

M. R. Conte; M. Morello; L. Mangiardi; F. Orzan; L. Checco; G. Bonfiglio; A. Alfarano; C. Camaschella; A. Brusca

An ARG403GLN β-myosin heavy chain gene mutation identified in an Italian family with hypertrophic cardiomyopathy: Description of clinical features of the family members [2]

M. R. Conte, M. Morello, L. Mangiardi, F. Orzan, L. Checco, G. Bonfiglio, A. Alfarano, C. Camaschella, A. Brusca

IRCCS Ospedale San Raffaele

Research output: Contribution to journal › Article

Original language	English
Pages (from-to)	1033-1034
Number of pages	2
Journal	European Heart Journal
Volume	18
Issue number	6
Publication status	Published - 1997

ASJC Scopus subject areas

Cardiology and Cardiovascular Medicine

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Conte, M. R., Morello, M., Mangiardi, L., Orzan, F., Checco, L., Bonfiglio, G., ... Brusca, A. (1997). An ARG403GLN β-myosin heavy chain gene mutation identified in an Italian family with hypertrophic cardiomyopathy: Description of clinical features of the family members [2]. European Heart Journal, 18(6), 1033-1034.

An ARG403GLN β-myosin heavy chain gene mutation identified in an Italian family with hypertrophic cardiomyopathy : Description of clinical features of the family members [2]. / Conte, M. R.; Morello, M.; Mangiardi, L.; Orzan, F.; Checco, L.; Bonfiglio, G.; Alfarano, A.; Camaschella, C.; Brusca, A.

In: European Heart Journal, Vol. 18, No. 6, 1997, p. 1033-1034.

Research output: Contribution to journal › Article

Conte, M. R. ; Morello, M. ; Mangiardi, L. ; Orzan, F. ; Checco, L. ; Bonfiglio, G. ; Alfarano, A. ; Camaschella, C. ; Brusca, A. / An ARG403GLN β-myosin heavy chain gene mutation identified in an Italian family with hypertrophic cardiomyopathy : Description of clinical features of the family members [2]. In: European Heart Journal. 1997 ; Vol. 18, No. 6. pp. 1033-1034.

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An ARG403GLN β-myosin heavy chain gene mutation identified in an Italian family with hypertrophic cardiomyopathy: Description of clinical features of the family members [2]

ASJC Scopus subject areas

Cite this

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