Fahr's disease linked to a novel mutation in MYORG variants manifesting as paroxysmal limb stiffness and dysarthria: Case report and literature review
ConclusionAll patients with primary brain calcification, particularly younger patients without a family history of the disease, should be screened forMYORG mutations.
Source: Molecular Genetics & Genomic Medicine - Category: Genetics & Stem Cells Authors: Tianxue Zhao,
Shaokun Xu,
Siyue Liu,
Juan Xu,
Xianfeng Zhang,
Yuhong Zhan Tags: CLINICAL REPORT Source Type: research