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

David J. Coote; Mark R. Davis; Macarena Cabrera; Merrilee Needham; Nigel G. Laing; Kristen J. Nowak

doi:10.1038/s41431-017-0065-3

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

David J. Coote, Mark R. Davis, Macarena Cabrera, Merrilee Needham, Nigel G. Laing, Kristen J. Nowak

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	1072-1077
Number of pages	6
Journal	European Journal of Human Genetics
Volume	26
Issue number	7
DOIs	https://doi.org/10.1038/s41431-017-0065-3
Publication status	Published - 1 Jul 2018

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10.1038/s41431-017-0065-3

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title = "Clinical Utility Gene Card for autosomal dominant myotonia congenita (Thomsen Disease)",

author = "Coote, {David J.} and Davis, {Mark R.} and Macarena Cabrera and Merrilee Needham and Laing, {Nigel G.} and Nowak, {Kristen J.}",

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AU - Laing, Nigel G.

AU - Nowak, Kristen J.

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

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NHMRC Research Fellowships - Laing

From Causative Genes to Establishing Therapies for Patients with Neuromuscular Diseases

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

Access to Document

Other files and links

Projects

NHMRC Research Fellowships - Laing

From Causative Genes to Establishing Therapies for Patients with Neuromuscular Diseases

Cite this