Dergiler / Turkish Journal of Hematology / 2020 / Cilt: 37 - Sayı: 2

A Novel Mutation in a Patient with Wiskott-Aldrich Syndrome

Sayfa
128–129
DOI
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Bu Makaleye Atıf Yap

ÖNCÜL, Y., AKYAY, A., TEKEDERELİ, İ. (2020). A Novel Mutation in a Patient with Wiskott-Aldrich Syndrome. Turkish Journal of Hematology, Cilt: 37 - Sayı: 2, 128–129. https://ajindex.com/articles/411540

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Kaynakça (7)

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  2. Ochs HD, Filipovich AH, Veys P, Cowan MJ, Kapoor N. Wiskott-Aldrich syndrome: diagnosis, clinical and laboratory manifestations, and treatment. Biol Blood Marrow Transplant 2009;15(1 Suppl):84-90
  3. Candotti F. Clinical manifestations and pathophysiological mechanisms of the Wiskott-Aldrich syndrome. J Clin Immunol 2018:38:13-27
  4. Notarangelo LD, Miao CH, Ochs HD. Wiskott-Aldrich syndrome. Curr Opin Hematol 2008;15:30-36
  5. Zhu Q, Zhang M, Blaese RM, Derry JM, Junker A, Francke U, Chen SH, Ochs HD. The Wiskott-Aldrich syndrome and X-linked congenital thrombocytopenia are caused by mutations of the same gene. Blood 1995;86:3797-3804
  6. Pelley JW. Elsevier’s Integrated Biochemistry, 2nd ed. Amsterdam, Elsevier, 2007
  7. Du W, Kumaki S, Uchiyama T, Yachie A, Yeng Looi C, Kawai S, Minegishi M, Ramesh N, Geha RS, Sasahara Y, Tsuchiya S. A second-site mutation in the initiation codon of WAS (WASP) results in expansion of subsets of lymphocytes in a Wiskott-Aldrich syndrome patient. Hum Mutat 2006;27:370-375.