Literature DB >> 23802135

Sequencing analysis of the ATOH7 gene in individuals with optic nerve hypoplasia.

Sing-Hui Lim1, Elizabeth St Germain, Khanh-Nhat Tran-Viet, Sandra Staffieri, Meghan Marino, Pr Hélène Dollfus, Erica B Nading, Sue Crowe, Glen Gole, Yaumara Perdomo-Trujillo, Michael Haybittel, James Elder, Valérie Pelletier, Elias Traboulsi, David Mackey, Terri L Young.   

Abstract

BACKGROUND: The Atonal Homolog 7 (ATOH7) gene has been implicated in association studies with optic nerve head diameter size. Hence, we screened optic nerve hypoplasia (ONH) patient DNA samples from Australia, France, and the United States for sequence variants in theATOH7 gene using Sanger sequencing.
METHODS: Sanger sequencing of theATOH7 gene was performed on 34 affected individual DNA samples. Sequencing was also carried out in three unaffected family members to confirm segregation of identified single nucleotide variations.
RESULTS: Seven sequence variations were identified in ATOH7. No disease-causing sequence changes in the ATOH7 gene was discovered in the ONH patient samples.
CONCLUSIONS: Mutations within the ATOH7 gene are not implicated in the pathogenesis of optic nerve hypoplasia in our patient cohort.

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Year:  2013        PMID: 23802135      PMCID: PMC4159081          DOI: 10.3109/13816810.2012.752017

Source DB:  PubMed          Journal:  Ophthalmic Genet        ISSN: 1381-6810            Impact factor:   1.803


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