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A novel MCM3AP mutation in a Lebanese family with recessive Charcot-Marie-Tooth neuropathy.
Kennerson, Marina L; Corbett, Alastair C; Ellis, Melina; Perez-Siles, Gonzalo; Nicholson, Garth A.
Affiliation
  • Kennerson ML; Northcott Neuroscience Laboratory, ANZAC Research Institute, Sydney, Australia.
  • Corbett AC; Sydney Medical School, University of Sydney, Sydney, Australia.
  • Ellis M; Molecular Medicine Laboratory, Concord Hospital, Sydney, Australia.
  • Perez-Siles G; Sydney Medical School, University of Sydney, Sydney, Australia.
  • Nicholson GA; Department of Neurology, Concord Hospital, Sydney, Australia.
Brain ; 141(9): e66, 2018 09 01.
Article in En | MEDLINE | ID: mdl-29982295
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Charcot-Marie-Tooth Disease / Intellectual Disability Limits: Humans Language: En Journal: Brain Year: 2018 Type: Article Affiliation country: Australia
Fulltext
Print
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Charcot-Marie-Tooth Disease / Intellectual Disability Limits: Humans Language: En Journal: Brain Year: 2018 Type: Article Affiliation country: Australia