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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
2007
2007
ABSTRACT Spinocerebellar ataxia type 10 (SCA10) is associated with expansion of (ATTCT)n repeats (where n is the number of… Expand
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Highly Cited
2006
Highly Cited
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
Review
2001
Review
2001
Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant progressive disorder characterized by ataxia, seizures and… Expand
1993
1993
On the basis of the three-dimensional structures of phospholipid and porcine pancreatic phospholipase A2 (pla2), it was predicted… Expand