Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian families.

Authors:
Ranieri M; Del Bo R; Bordoni A; Ronchi D; Colombo I and 8 more

Journal:
J Neurol Sci

Publication Year: 2011

DOI:
10.1016/j.jns.2011.12.002

PMCID:
PMC3315002

PMID:
22197506

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Journal Information

Full Title: J Neurol Sci

Abbreviation: J Neurol Sci

Country: Unknown

Publisher: Unknown

Language: N/A

Publication Details

Subject Category: Neurology

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

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"Conflict of interest The authors report no competing interests."

Evidence found in paper:

"Funding The financial support of the following research grant is gratefully acknowledged: Telethon-UILDM Project GUP09004 “Construction of a database for a nation wide Italian collaborative network of mitochondrial diseases”, Associazione Amici del Centro Dino Ferrari, University of Milan, the Telethon project GTB07001, the Eurobiobank project QLTR-2001-02769 and R.F. 02.187 Criobanca Automatizzata di Materiale Biologico."

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