Indentification of novel MSTO1 compound heterozygous mutations in a Chinese family with recessive cerebellar atrophy and ataxia

Indentification of novel MSTO1 compound heterozygous mutations in a Chinese family with recessive cerebellar atrophy and ataxia https://t.co/MR4HuWnvDw https://t.co/Vjg6ZoR4pd

New Research: Indentification of novel MSTO1 compound heterozygous mutations in a Chinese family with recessive cerebellar atrophy and ataxia: Misato mitochondrial distribution and morphology regulator 1 (MSTO1) is a nuclear-encoded… https://t.co/EtRltFPNv