Title : Microglial Activation in the Pathogenesis of Huntington's Disease.

Pub. Date : 2017

PMID : 28674491






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Huntington"s disease (HD) is an autosomal dominantly inherited neurodegenerative disorder caused by expanded CAG trinucleotide repeats (>36) in exon 1 of HTT gene that encodes huntingtin protein. trinucleotide huntingtin Homo sapiens
2 Huntington"s disease (HD) is an autosomal dominantly inherited neurodegenerative disorder caused by expanded CAG trinucleotide repeats (>36) in exon 1 of HTT gene that encodes huntingtin protein. trinucleotide huntingtin Homo sapiens