Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

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Volume
38
Pagination
1242 - 1244
DOI
10.1038/ng1893
Journal
NAT GENET
Issue
11
ISSN
1061-4036
Metadata
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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/jspui/handle/123456789/7467
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