Fourteen novel OPA1 mutations in autosomal dominant optic atrophy including two de novo mutations in sporadic optic atrophy
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B. Lorenz | D. Bonneau | P. Amati‐Bonneau | P. Reynier | H. Dollfus | P. Jonveaux | S. Mohammed | C. Ayuso | C. Hamel | I. Maumenee | Olivier R Baris | C. Delettre | M. Surget | J. Charlin | A. Catier | L. Derieux | J. Guyomard | Y. Tourmen | Y. Malthiéry