ATXN10 gene

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

Topic mentions per year

Topic mentions per year

1993-2018
01219932018

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2018
Review
2018
Microdeletion of chromosome 22q13.31 is a very rare condition. Fourteen patients have been annotated in public databases but, to… (More)
Is this relevant?
2017
2017
Large, non-coding pentanucleotide repeat expansions of ATTCT in intron 9 of the ATXN10 gene typically cause progressive… (More)
  • figure 1
  • figure 2
  • table 1
  • figure 3
  • figure 4
Is this relevant?
2016
2016
Chlamydia trachomatis is the leading causative agent of bacterial sexually transmitted infections worldwide which can lead to… (More)
Is this relevant?
2010
2010
We have identified a large expansion of an ATTCT repeat within intron 9 of ATXN10 on chromosome 22q13.31 as the genetic mutation… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
2009
2009
Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant neurodegenerative disorder characterized by ataxia and cerebellar… (More)
  • figure 1
Is this relevant?
2007
2007
Spinocerebellar ataxia type 10 (SCA10) is associated with expansion of (ATTCT)n repeats (where n is the number of repeats) within… (More)
Is this relevant?
2006
2006
BACKGROUND Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant disorder characterized by cerebellar ataxia and… (More)
Is this relevant?
2006
2006
Spinocerebellar ataxia type 10 (SCA10) is a dominantly inherited disorder caused by an intronic ATTCT pentanucleotide repeat… (More)
Is this relevant?
Review
2005
Review
2005
Spinocerebellar ataxia type 10 (SCA10) is a dominantly inherited ataxia caused by expansion of ATTCT pentanucleotide repeat in… (More)
Is this relevant?
1993
1993
On the basis of the three-dimensional structures of phospholipid and porcine pancreatic phospholipase A2 (pla2), it was predicted… (More)
Is this relevant?