Title : Progressive retinal degeneration and dysfunction in R6 Huntington's disease mice.

Pub. Date : 2002 Dec 15

PMID : 12471061






4 Functional Relationships(s)
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1 Huntington"s disease (HD) and spinocerebellar ataxia type 7 (SCA7) belong to a group of progressive neurodegenerative diseases caused by polyglutamine (polyQ) expansions. polyglutamine ataxin 7 Mus musculus
2 Huntington"s disease (HD) and spinocerebellar ataxia type 7 (SCA7) belong to a group of progressive neurodegenerative diseases caused by polyglutamine (polyQ) expansions. polyglutamine ataxin 7 Mus musculus
3 Huntington"s disease (HD) and spinocerebellar ataxia type 7 (SCA7) belong to a group of progressive neurodegenerative diseases caused by polyglutamine (polyQ) expansions. polyglutamine ataxin 7 Mus musculus
4 Huntington"s disease (HD) and spinocerebellar ataxia type 7 (SCA7) belong to a group of progressive neurodegenerative diseases caused by polyglutamine (polyQ) expansions. polyglutamine ataxin 7 Mus musculus