Clinical Utility Gene Card for: Autosomal dominant myotonia congenita (Thomsen Disease)

Journal article

Peer reviewed

D.J. Coote, M.R. Davis, M. Cabrera, M. Needham, N.G. Laing and K.J. Nowak

European Journal of Human Genetics, Vol.26, pp.1072-1077

2018

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Title: Clinical Utility Gene Card for: Autosomal dominant myotonia congenita (Thomsen Disease)
Authors/Creators: D.J. Coote (Author/Creator)
M.R. Davis (Author/Creator)
M. Cabrera (Author/Creator)
M. Needham (Author/Creator)
N.G. Laing (Author/Creator)
K.J. Nowak (Author/Creator)
Publication Details: European Journal of Human Genetics, Vol.26, pp.1072-1077
Publisher: Springer Nature
Identifiers: 991005543804607891
Copyright: © 2018 Macmillan Publishers Limited, part of Springer Nature
Murdoch Affiliation: Murdoch University
Language: English
Resource Type: Journal article

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Collaboration types: Domestic collaboration; International collaboration
Citation topics: 1 Clinical & Life Sciences; 1.79 Molecular & Cell Biology - Physiology; 1.79.1811 Myotonic Dystrophy Mechanisms
Web Of Science research areas: Biochemistry & Molecular Biology; Genetics & Heredity
ESI research areas: Molecular Biology & Genetics