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Wiskott–Aldrich syndrome: review and report of a large family

Wiskott–Aldrich syndrome is a sex-linked recessive antibody-deficiency syndrome characterized by thrombocytopenia, eczema and increased susceptibility to infection. All forms of therapy are notably unsuccessful and these patients succumb in the first decade. Three cases of this syndrome are presente...

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Hlavní autoři: Stiehm, E. R., McIntosh, R. M.
Médium: Artigo
Jazyk:Inglês
Vydáno: 1967
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1578833/
https://ncbi.nlm.nih.gov/pubmed/4166240
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