Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus (Q24651919)

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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 (English)
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    Konstantinos Droutsas

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