Reverse phenotyping to further define a new mitochondrial depletion syndrome caused by an ISCA2 mutation Commentary on: Alfadhel et al. Further delineation of the phenotypic spectrum of ISCA2 defect: A report of ten new cases-MedSci.cn

Reverse phenotyping to further define a new mitochondrial depletion syndrome caused by an ISCA2 mutation Commentary on: Alfadhel et al. Further delineation of the phenotypic spectrum of ISCA2 defect: A report of ten new cases

Babiker, MOE

Babiker, MOE (reprint author), Bristol Royal Hosp Children, Bristol, Avon, England.

EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, 2018; 22 (1): 4

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