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

✍ Scribed by K. Zhang; J. A. Johnson; J. Biroschak; J. Villanueva; S. Molleran Lee; J. J. Bleesing; K. A. Risma; R. J. Wenstrup; A. H. Filipovich


Book ID
114831429
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
90 KB
Volume
34
Category
Article
ISSN
1744-3121

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