Next generation sequencing in family with MNGIE syndrome associated to optic atrophy: Novel homozygous POLG mutation in the C-terminal sub-domain leading to mtDNA depletion.
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C. Bris | D. Goudenège | V. Desquiret-Dumas | Majida Charif | D. Bonneau | P. Amati‐Bonneau | G. Lenaers | P. Reynier | V. Procaccio | F. Fakhfakh | M. Hachicha | R. Felhi | L. Ammar-keskes | L. Sfaihi | M. Charif