Identification of three novel OA1 gene mutations identified in three families misdiagnosed with congenital nystagmus and carrier status determination by real-time quantitative PCR assay.

Authors:
Faugère V; Tuffery-Giraud S; Hamel C; Claustres M.

Journal:
BMC Genet

Publication Year: 2003

DOI:
10.1186/1471-2156-4-1

PMCID:
PMC140306

PMID:
12515581

Journal Information

Journal Title: BMC Genet

Detailed journal information not available.

Publication Details

Subject Category: Genetics & Heredity

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

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Last Updated: Aug 05, 2025