A novel mutation of AFG3L2 might cause dominant optic...

Frontiers in Genetics 2015 / 10 Vol. 6

A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disability

Charif, Majida, Roubertie, Agathe, Salime, Sara, Mamouni, Sonia, Goizet, Cyril, Hamel, Christian P., Lenaers, Guy
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Volume:
6
Language:
english
Journal:
Frontiers in Genetics
DOI:
10.3389/fgene.2015.00311
Date:
October, 2015
File:
PDF, 1.18 MB
english, 2015
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