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

✍ Scribed by Tarpey, Patrick; Thomas, Shery; Sarvananthan, Nagini; Mallya, Uma; Lisgo, Steven; Talbot, Chris J; Roberts, Eryl O; Awan, Musarat; Surendran, Mylvaganam; McLean, Rebecca J

Book ID: 109919442
Publisher: Nature Publishing Group
Year: 2006
Tongue: English
Weight: 181 KB
Volume: 38
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng1893

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