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    Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus 
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    • Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus
    •   QMRO Home
    • Blizard Institute
    • Centre for Genomics and Child Health
    • Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus
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    Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

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    Published version (180.7Kb)
    Volume
    38
    Pagination
    1242 - 1244
    DOI
    10.1038/ng1893
    Journal
    NAT GENET
    Issue
    11
    ISSN
    1061-4036
    Metadata
    Show full item record
    Authors
    Tarpey, P; Thomas, S; Sarvananthan, N; Mallya, U; Lisgo, S; Talbot, CJ; Roberts, EO; Awan, M; Surendran, M; McLean, RJ
    URI
    http://qmro.qmul.ac.uk/xmlui/handle/123456789/7467
    Collections
    • Centre for Genomics and Child Health [659]
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