Genotype phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations-Reference-Cited by-同舟云学术

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Genotype phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations

Published:2007-10-26 Issue:1 Volume:45 Page:15-21
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Trizzino A,Stadt U z.,Ueda I,Risma K,Janka G,Ishii E,Beutel K,Sumegi J,Cannella S,Pende D,Mian A,Henter J-I,Griffiths G,Santoro A,Filipovich A,Arico M,

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Cited by 118 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Evaluating whole genome sequencing for rare diseases in newborn screening: evidence synthesis from a series of systematic reviews;2024-09-04

2. Genetic background of primary and familial HLH in Qatar: registry data and population study;Frontiers in Pediatrics;2024-05-09

3. Precise CRISPR-Cas9 gene repair in autologous memory T cells to treat familial hemophagocytic lymphohistiocytosis;Science Immunology;2024-02-02

4. Hemophagocytic Lymphohistiocytosis in Adolescents and Young Adults;Medical Clinics of North America;2024-01

5. Hemophagocytic lymphohistiocytosis with a hemizygous PRF1 c.674G>A mutation;The American Journal of the Medical Sciences;2023-11

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