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SH2D1A mutation analysis for diagnosis of XLP in typical and atypical patients

L. Yin; V. Ferrand; M.-F. Lavou�; D. Hayoz; N. Philippe; G. Souillet; M. Seri; R. Giacchino; E. Castagnola; S. Hodgson; B.S. Sylla; G. Romeo
Human Genetics · Vol. 105, Issue 5 · pp. 501-505 · 1999
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Bibliographic Information

JournalHuman Genetics
PublisherSpringer
Publication Date1999-11-15
Publication Year1999
Volume105
Issue5
Pages501-505
Document TypeJournal Article
Print ISSN0340-6717
eISSN1432-1203
DOI10.1007/s004390051137

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NARA Access Coverage1964-01-01~Current
Journal Homepagehttps://www.springer.com/journal/439
Publisher PageOpen Publisher Page
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