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No mutation of elastin and fibulin-5 genes in a patient with acquired cutis laxa associated with chronic urticaria

✍ Scribed by X.-K. Sun; J.-F. Chen


Book ID
108671460
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
412 KB
Volume
164
Category
Article
ISSN
0007-0963

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## Abstract Recently, mutations of two genes, SAP/SH2D1A/DSHP and perforin genes, have been identified in two fatal inherited lymphoproliferative diseases, X‐linked lymphoproliferative disease and familial hemophagocytic lymphohistiocytosis, respectively. Epstein‐Barr virus (EBV)‐associated hemopha