Genotype–phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations | Journal of Medical Genetics

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Genotype–phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations

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Cite this article as:: Trizzino A, Stadt UZ, Ueda I, et al

Genotype–phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations

Journal of Medical Genetics 2008;45:15-21.