Title : Clinical and molecular characteristics of a Brazilian family with spinocerebellar ataxia type 1.

Pub. Date : 1996 Sep

PMID : 9109985






2 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 Expansions of an unstable trinucleotide CAG repeat cause three of these disorders: SCA1, MJD/SCA3 and DRPLA. trinucleotide ataxin 3 Homo sapiens
2 Expansions of an unstable trinucleotide CAG repeat cause three of these disorders: SCA1, MJD/SCA3 and DRPLA. trinucleotide ataxin 3 Homo sapiens