False-positive SCA8 Gene Test in a Patient with Pathologically Proven Multiple System Atrophy
Overview
Affiliations
The Frequency of Intermediate Alleles in Patients with Cerebellar Phenotypes.
Capacci E, Bagnoli S, Giacomucci G, Rapillo C, Govoni A, Bessi V Cerebellum. 2023; 23(3):1135-1145.
PMID: 37906407 PMC: 11102406. DOI: 10.1007/s12311-023-01620-7.
The genetic basis of multiple system atrophy.
Tseng F, Foo J, Mai A, Tan E J Transl Med. 2023; 21(1):104.
PMID: 36765380 PMC: 9912584. DOI: 10.1186/s12967-023-03905-1.
Clinical and neuroimaging review of triplet repeat diseases.
Kurokawa R, Kurokawa M, Mitsutake A, Nakaya M, Baba A, Nakata Y Jpn J Radiol. 2022; 41(2):115-130.
PMID: 36169768 PMC: 9889482. DOI: 10.1007/s11604-022-01343-5.
The First Case of Spinocerebellar Ataxia Type 8 in Monozygotic Twins.
Sawada J, Katayama T, Tokashiki T, Kikuchi S, Kano K, Takahashi K Intern Med. 2019; 59(2):277-283.
PMID: 31554751 PMC: 7008061. DOI: 10.2169/internalmedicine.2905-19.
Genetic and clinical analyses of spinocerebellar ataxia type 8 in mainland China.
Zhou Y, Yuan Y, Liu Z, Zeng S, Chen Z, Shen L J Neurol. 2019; 266(12):2979-2986.
PMID: 31471687 DOI: 10.1007/s00415-019-09519-2.