OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance.
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E. Zrenner | B. Jurklies | B. Wissinger | U. Pesch | B. Leo-Kottler | S. Mayer | U. Kellner | E. Apfelstedt-Sylla | C. Alexander | U. E. Pesch | E. Apfelstedt‐Sylla | Eberhart Zrenner | Simone Mayer | Ulrich Kellner