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T-cell Acute Lymphoblastic Leukemia in Association with Börjeson-Forssman-Lehmann Syndrome Due to a Mutation in PHF6
Börjeson-Forssman-Lehmann syndrome (BFLS) is a rare X-linked mental retardation syndrome that is caused by germline mutations in PHF6. We describe a 9-year old male with BFLS, who developed T-cell acute lymphoblastic leukemia (T-ALL). The PHF6 gene is located on the X chromosome and encodes a protei...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2933084/ https://ncbi.nlm.nih.gov/pubmed/20806366 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/pbc.22574 |
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