A neonatal polyvisceral failure linked to a de novo homoplasmic mutation in the mitochondrially encoded cytochrome b gene.
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V. Procaccio | P. Potluri | S. Bannwarth | J. Lambert | V. Serre | K. Fragaki | C. Caruba | Sean F. O’Hearn | Gaëlle Augé | F. Casagrande | V. Paquis-Flucklinger