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Article

Familial haemophagocytic lymphohistiocytosis in patients who are heterozygous for the A91V perforin variation is often associated with other genetic defects.

International journal of immunogenetics - 1 Aug 2007

Zhang K, Johnson J A, Biroschak J, Villanueva J, Lee S Molleran, Bleesing J J, Risma K A, Wenstrup R J, Filipovich A H

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 17627755
DOI: 10.1111/j.1744-313X.2007.00679.x

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Familial haemophagocytic lymphohistiocytosis in patients who are heterozygous for the A91V perforin variation is often associated with other genetic defects.PMID 17627755Read ↗

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