K Goransdotter Ericson
Overview
Explore the profile of K Goransdotter Ericson including associated specialties, affiliations and a list of published articles.
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Articles
2
Citations
92
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Recent Articles
1.
Rudd E, Goransdotter Ericson K, Zheng C, Uysal Z, Ozkan A, Gurgey A, et al.
J Med Genet
. 2006 Apr;
43(4):e14.
PMID: 16582076
Objective: To determine the frequency and spectrum of mutations in the gene encoding syntaxin 11 (STX11) in familial haemophagocytic lymphohistiocytosis (FHL), a rare autosomal recessive disorder of immune dysregulation characterised...
2.
Goransdotter Ericson K, Fadeel B, Nilsson-Ardnor S, Soderhall C, Samuelsson A, Janka G, et al.
Am J Hum Genet
. 2001 Feb;
68(3):590-7.
PMID: 11179007
Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal recessive disease of early childhood characterized by nonmalignant accumulation and multivisceral infiltration of activated T lymphocytes and histiocytes (macrophages). Cytotoxic T and natural...