A family with 2 X-linked disorders: Charcot-Marie-Tooth disease and hemophilia A
Nortina Shahrizaila DM, FRCP
Division of Neurology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia
Search for more papers by this authorKhean Jin Goh FRCP
Division of Neurology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia
Search for more papers by this authorAzlina Ahmad-Annuar PhD
Department of Molecular Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia
Search for more papers by this authorRabia Chaudhry BSc
Northcott Neuroscience Laboratory, ANZAC Research Institute and Sydney Medical School, University of Sydney, Sydney, Australia
Search for more papers by this authorCarolyn Ly BSc
Northcott Neuroscience Laboratory, ANZAC Research Institute and Sydney Medical School, University of Sydney, Sydney, Australia
Search for more papers by this authorMonique M. Ryan MMed
Children's Neuroscience Centre, Royal Children's Hospital, Victoria, Australia
Search for more papers by this authorGarth Nicholson PhD
Northcott Neuroscience Laboratory, ANZAC Research Institute and Sydney Medical School, University of Sydney, Sydney, Australia
Search for more papers by this authorMarina Kennerson PhD
Northcott Neuroscience Laboratory, ANZAC Research Institute and Sydney Medical School, University of Sydney, Sydney, Australia
Search for more papers by this authorNortina Shahrizaila DM, FRCP
Division of Neurology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia
Search for more papers by this authorKhean Jin Goh FRCP
Division of Neurology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia
Search for more papers by this authorAzlina Ahmad-Annuar PhD
Department of Molecular Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia
Search for more papers by this authorRabia Chaudhry BSc
Northcott Neuroscience Laboratory, ANZAC Research Institute and Sydney Medical School, University of Sydney, Sydney, Australia
Search for more papers by this authorCarolyn Ly BSc
Northcott Neuroscience Laboratory, ANZAC Research Institute and Sydney Medical School, University of Sydney, Sydney, Australia
Search for more papers by this authorMonique M. Ryan MMed
Children's Neuroscience Centre, Royal Children's Hospital, Victoria, Australia
Search for more papers by this authorGarth Nicholson PhD
Northcott Neuroscience Laboratory, ANZAC Research Institute and Sydney Medical School, University of Sydney, Sydney, Australia
Search for more papers by this authorMarina Kennerson PhD
Northcott Neuroscience Laboratory, ANZAC Research Institute and Sydney Medical School, University of Sydney, Sydney, Australia
Search for more papers by this authorReferences
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- 4 Kennerson M, Nicholson G, Kowalski B, et al. X-linked distal hereditary motor neuropathy maps to the DSMAX locus on chromosome Xq13.1-q21. Neurology 2009; 72: 246–252
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