Clinical, Molecular, and Computational Analysis in two cases with mitochondrial encephalomyopathy associated with SUCLG1 mutation in a consanguineous family.
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F. Fakhfakh | J. Bouguila | L. Boughamoura | L. Keskes | A. Tej | S. Majdoub | R. Felhi | Boudour Khabou | E. Mkaouar-Rebai | M. Maalej | Marwa Ammar | S. Tilouche | Mouna Tabbebi