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ATXN10 gene

Known as: E46L, ATXN10, E46-LIKE 
 
National Institutes of Health

Papers overview

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2017
2017
Large, non-coding pentanucleotide repeat expansions of ATTCT in intron 9 of the ATXN10 gene typically cause progressive… Expand
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2013
2013
The flavivirus nonstructural protein 5 (NS5) is a large protein that is structurally conserved among members of the genus, making… Expand
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Highly Cited
2010
Highly Cited
2010
We have identified a large expansion of an ATTCT repeat within intron 9 of ATXN10 on chromosome 22q13.31 as the genetic mutation… Expand
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Review
2008
Review
2008
Spinocerebellar ataxia type 10 (SCA10) is a dominantly inherited ataxia caused by expansion of ATTCT pentanucleotide repeat in… Expand
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2007
2007
Spinocerebellar ataxia type 10 (SCA10) is associated with expansion of (ATTCT)n repeats (where n is the number of repeats) within… Expand
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2006
2006
Background:Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant disorder characterized by cerebellar ataxia and… Expand
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2006
2006
Spinocerebellar ataxia type 10 (SCA10) is a dominantly inherited disorder caused by an intronic ATTCT pentanucleotide repeat… Expand
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Review
2001
Review
2001
Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant progressive disorder characterized by ataxia, seizures and… Expand
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1993
1993
On the basis of the three-dimensional structures of phospholipid and porcine pancreatic phospholipase A2 (pla2), it was predicted… Expand
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