Title : Clinical phenotype in carriers of intermediate alleles in the huntingtin gene.

Pub. Date : 2019 Jul 15

PMID : 31103960






1 Functional Relationships(s)
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1 BACKGROUND: Huntington disease (HD) is caused by a mutation in the HTT gene of 36 or more CAG trinucleotide repeats. trinucleotide huntingtin Homo sapiens