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Investigation of calmodulin-like and rod domain mutations suggests common molecular mechanism for α-actinin-1-linked congenital macrothrombocytopenia.
O'Sullivan, Leanne Rose; Ajaykumar, Amarendra Praburam; Dembicka, Kornelia Maria; Murphy, Aidan; Grennan, Eamonn Paul; Young, Paul William.
Affiliation
  • O'Sullivan LR; School of Biochemistry and Cell Biology, Western Gateway Building, University College Cork, Cork, Ireland.
  • Ajaykumar AP; School of Biochemistry and Cell Biology, Western Gateway Building, University College Cork, Cork, Ireland.
  • Dembicka KM; School of Biochemistry and Cell Biology, Western Gateway Building, University College Cork, Cork, Ireland.
  • Murphy A; School of Biochemistry and Cell Biology, Western Gateway Building, University College Cork, Cork, Ireland.
  • Grennan EP; School of Biochemistry and Cell Biology, Western Gateway Building, University College Cork, Cork, Ireland.
  • Young PW; School of Biochemistry and Cell Biology, Western Gateway Building, University College Cork, Cork, Ireland.
FEBS Lett ; 594(1): 161-174, 2020 01.
Article in En | MEDLINE | ID: mdl-31365757
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thrombocytopenia / Actinin / Mutation, Missense Limits: Animals / Humans Language: En Journal: FEBS Lett Year: 2020 Document type: Article Affiliation country: Country of publication:
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thrombocytopenia / Actinin / Mutation, Missense Limits: Animals / Humans Language: En Journal: FEBS Lett Year: 2020 Document type: Article Affiliation country: Country of publication: