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Human perforin gene variation is geographically distributed
BACKGROUND: Deleterious mutations in PRF1 result in lethal, childhood disease, familial hemophagocytic lymphohistiocytosis type 2 (FHL 2). However, not all mutations in PRF1 are deleterious and result in FHL 2. Currently, these nondeleterious mutations are being investigated in the onset of numerous...
Autores principales: | Willenbring, Robin C., Ikeda, Yasuhiro, Pease, Larry R., Johnson, Aaron J. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5823683/ https://www.ncbi.nlm.nih.gov/pubmed/29216683 http://dx.doi.org/10.1002/mgg3.344 |
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