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

被引：0
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作者：
David J. Coote
Mark R. Davis
Macarena Cabrera
Merrilee Needham
Nigel G. Laing
Kristen J. Nowak
机构：
[1] The University of Western Australia; and Harry Perkins Institute of Medical Research,Centre for Medical Research, Faculty of Health and Medical Sciences
[2] PP Block,Neurogenetics Laboratory, Department of Diagnostic Genomics
[3] QEII Medical Centre,Department of Neurology and Instituto de Biomedicina de Sevilla
[4] Hospital Universitario Virgen del Rocío,Western Australian Neuroscience Institute
[5] QEII Medical Centre,School of Biomedical Sciences, Faculty of Health and Medical Sciences
[6] Nedlands,undefined
[7] Western Australia 6009; Fiona Stanley Hospital,undefined
[8] The University of Western Australia,undefined
[9] Office of Population Health Genomics,undefined
[10] Public and Aboriginal Health Division,undefined
[11] Department of Health,undefined
来源：
European Journal of Human Genetics | 2018年 / 26卷
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页码：1072 / 1077
页数：5
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