Associated Papers
Fahr's disease linked to a novel mutation in MYORG variants manifesting as paroxysmal limb stiffness and dysarthria: Case report and literature review.
Zhao T et al.
Molecular Genetics & Genomic Medicine, 2023
The primary familial brain calcification-associated protein MYORG is an α-galactosidase with restricted substrate specificity.
Meek RW et al.
Plos Biology, 2022
36129849 (PubMed )
Supplement: pbio.3001764.s007.pdf
Paroxysmal Kinesigenic Dyskinesia Secondary to Brain Calcification with a Homozygous MYORG Mutation.
Du J et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2021
MYORG Mutations: a Major Cause of Recessive Primary Familial Brain Calcification.
Bauer M et al.
Current Neurology and Neuroscience Reports, 2019
Biallelic MYORG mutation carriers exhibit primary brain calcification with a distinct phenotype.
Grangeon L et al.
Brain : a Journal of Neurology, 2019
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