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.

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. Eur J Paediatr Neurol. 2017 Dec 21;: Authors: Babiker MOE PMID: 29289521 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/29289521?dopt=Abstract

Source: European Journal of Paediatric Neurology - December 21, 2017 Category: Neurology Authors: Babiker MOE Tags: Eur J Paediatr Neurol Source Type: research

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