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Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.
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- 2011
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- Correction Notice
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.
- Published in:
- Nature Genetics, 2006, v. 38, n. 11, p. 1242, doi. 10.1038/ng1893
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- Publication type:
- Article
Phenotypical characteristics of idiopathic infantile nystagmus with and without mutations in FRMD7.
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- Brain: A Journal of Neurology, 2008, v. 131, n. 5, p. 1259, doi. 10.1093/brain/awn046
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- Article