Title : A human huntingtin SNP alters post-translational modification and pathogenic proteolysis of the protein causing Huntington disease.

Pub. Date : 2018 May 25

PMID : 29802276






2 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 Huntington disease (HD) is a dominantly inherited neurodegenerative disorder caused by an expanded CAG trinucleotide repeat in the huntingtin (HTT) gene. trinucleotide huntingtin Homo sapiens
2 Huntington disease (HD) is a dominantly inherited neurodegenerative disorder caused by an expanded CAG trinucleotide repeat in the huntingtin (HTT) gene. trinucleotide huntingtin Homo sapiens