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A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy

✍ Scribed by E. Cardaioli; G. N. Gallus; P. Da Pozzo; A. Rufa; R. Franceschini; E. Motolese; A. Caporossi; M. T. Dotti; A. Federico


Publisher
Springer
Year
2005
Tongue
English
Weight
202 KB
Volume
253
Category
Article
ISSN
0340-5354

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