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CCT3 gene

Known as: CHAPERONIN CONTAINING TCP1, SUBUNIT 3, CCT-GAMMA, CCTG 
 
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
BACKGROUND PAPA syndrome is a recently identified hereditary autoinflammatory syndrome clinically characterized by pyogenic… Expand
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Highly Cited
2009
Highly Cited
2009
Myotonic dystrophy (DM) is a genetic disorder caused by the expression (as RNA) of expanded CTG or CCTG repeats. The alternative… Expand
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Review
2005
Review
2005
  • E. Nanba
  • Nihon rinsho. Japanese journal of clinical…
  • 2005
  • Corpus ID: 1477934
Myotonic dystrophy is a dominantly inherited disorder with multisystemic clinical features affecting skeletal muscle, the heart… Expand
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Review
2004
Review
2004
  • L. Ranum, J. Day
  • American journal of human genetics
  • 2004
  • Corpus ID: 44926186
Myotonic dystrophy (DM)--the most common form of muscular dystrophy in adults, affecting 1/8000 individuals--is a dominantly… Expand
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Highly Cited
2004
Highly Cited
2004
Myotonic dystrophy (DM) is caused by either an untranslated CTG expansion in the 3' untranslated region of the DMPK gene on… Expand
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Highly Cited
2003
Highly Cited
2003
Background: Myotonic dystrophy types 1 (DM1) and 2 (DM2/proximal myotonic myopathy PROMM) are dominantly inherited disorders with… Expand
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Highly Cited
2003
Highly Cited
2003
Myotonic dystrophy type 1 (DM1) and type 2 (DM2) are caused by genomic expansions of CTG or CCTG repeats. When transcribed, these… Expand
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Highly Cited
2002
Highly Cited
2002
Myotonic dystrophy is a complex neuromuscular disorder associated with DNA expansion mutations in two different genes. In DM1 a… Expand
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Highly Cited
2001
Highly Cited
2001
Myotonic dystrophy (DM), the most common form of muscular dystrophy in adults, can be caused by a mutation on either chromosome… Expand
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Highly Cited
1994
Highly Cited
1994
BACKGROUND TCP-1 is a 60 kD subunit of a cytosolic hetero-oligomeric chaperone that is known to be involved in the folding of… Expand
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