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PPP2R1A wt Allele

Known as: PR65A, Protein Phosphatase 2 (Formerly 2A), Regulatory Subunit A (PR 65), Alpha Isoform Gene, Protein Phosphatase 2, 65kDa Regulatory Subunit A Gene 
Human PPP2R1A wild-type allele is located in the vicinity of 19q13.41 and is approximately 37 kb in length. This allele, which encodes serine… Expand
National Institutes of Health

Papers overview

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2013
2013
Previously, we identified the genetic variant −241 (−/G) (rs11453459) in the PP2A-Aα gene (PPP2R1A) promoter and demonstrated… Expand
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2010
2010
Hereditary dysfibrinogenemia is a rare clotting disorder, which results from mutations in at least one of the three fibrinogen… Expand
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2007
2007
We detail for the first time the uniquely altered fibrin polymerization of homophenotypic Aα R16H dysfibrinogen. By polymerase… Expand
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2007
2007
INTRODUCTION Various dysfibrinogenemias have been described worldwide. This paper describes two new cases of dysfibrinogenemia… Expand
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2004
2004
Summary.  Fibrinogen Lima is an abnormal fibrinogen with an Aα Arg141→Ser substitution resulting in an extra N‐glycosylation at A… Expand
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2001
2001
Fibrinogen Milano XII was detected in an asymptomatic Italian woman, whose routine coagulation test results revealed a prolonged… Expand
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2001
2001
Fibrinogen Milano XII was detected in an asymptomatic Italian woman, whose routine coagulation test results revealed a prolonged… Expand
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