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Family Studies of WHIM Syndrome
PURPOSE OF THE REVIEW: WHIM syndrome (warts, hypogammaglobulinemia, immunodeficiency, myelokathexis, or WHIMs) is a very rare autosomal dominant immunodeficiency disorder attributable to mutations in CXCR4. We reviewed clinical manifestations in 24 patients in 9 families to expand understanding of t...
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| Publicado no: | Curr Opin Hematol |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7241424/ https://ncbi.nlm.nih.gov/pubmed/31652152 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MOH.0000000000000554 |
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