Associated Papers
MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1.
Flower M et al.
Brain : a Journal of Neurology, 2019
Clinical manifestations of homozygote allele carriers in Huntington disease.
Cubo E et al.
Neurology, 2019
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.
Moss DJH et al.
The Lancet. Neurology, 2017
De Novo Occurrence of a Variant in ARL3 and Apparent Autosomal Dominant Transmission of Retinitis Pigmentosa.
Strom SP et al.
Plos One, 2016
26964041 (PubMed )
Supplement: pone.0150944.s002.xls › All_variants
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