Article
Radiologic manifestation of a BCS1L-mutated patient.
Journal of pediatric endocrinology & metabolism : JPEM - 1 Mar 2014
Özmen Evrim, Ünlü Havva Akmaz, Demirkan Tülin Hakan, Tiftik Mehmet, Adaletli İbrahim
Abstract excerpt
There are various phenotypes of mutations in BCS1L which encode a mitochondrial inner membrane protein that facilitates the insertion of Rieske iron-sulfur protein into respiratory chain complex III. Herein we report the radiologic findings of a patient with bc1 synthesis-like (BCS1L) gene mutation who was presented with convulsions.
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