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Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations.

Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations. Research Abstract Details 

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  • Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations. Abstract Text:

    d zhuD Zhu,m l kennersonM L Kennerson,g walizadaG Walizada,s S ,j m vanceJ M Vance,g a nicholsonG A Nicholson,

    Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations. Publishing Authors By Initials

    d zhuD Zhu,ml kennersonML Kennerson,g walizadaG Walizada,s S ,jm vanceJM Vance,ga nicholsonGA Nicholson,

    For similar genetic phenomena: variation (genetics) research abstracts see: genetic phenomena: variation (genetics) research

    PUBMED ID PMID:

    MEDLINE DATE:

    Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Neurology

    VOLUME: 65

    Page Numbers: 496-7

    Journal Abbreviation: Neurology

    ISSN: 1526-632X

    DAY: 9

    MONTH: Aug

    YEAR: 2005

    Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 401060

    Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations. Keywords Mesh Terms:

    KEYWORDS: Variation (Genetics)

    MESH TERMS: genetics

    Chemical & Substance for Abstract: Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations. Information

    Substance Name: Kinesin

    Registry Number: EC 3.6.1.-

    Grant and Affiliation Information for Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations.

    AFFILIATION: ANZAC Research Institute, University of Sydney, Concord Hospital, NSW, Australia. danqing@med.usyd.edu.au

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY:

    GRANT:

    ACRONYM:

    MEDLINETA: Neurology

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

    Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations Related Publications

     

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