Title : Proteomics of Huntington's disease-affected human embryonic stem cells reveals an evolving pathology involving mitochondrial dysfunction and metabolic disturbances.

Pub. Date : 2014 Dec 5

PMID : 25316320






2 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 Huntington"s disease (HD) is an autosomal dominant neurodegenerative disorder caused by a mutation in the Huntingtin gene, where excessive (>= 36) CAG repeats encode for glutamine expansion in the huntingtin protein. Glutamine huntingtin Homo sapiens
2 Huntington"s disease (HD) is an autosomal dominant neurodegenerative disorder caused by a mutation in the Huntingtin gene, where excessive (>= 36) CAG repeats encode for glutamine expansion in the huntingtin protein. Glutamine huntingtin Homo sapiens