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Central nervous system involvement in a case of familial hemophagocytic lymphohistiocytosis with perforin mutation.
Akbayram, S; Akgun, C; Dogan, M; Caksen, H; Okur, H; Oner, A F.
Affiliation
  • Akbayram S; Yuzuncu Yil University, Faculty of Medicine, Division of Pediatric Hematology, Van, Turkey. drsinanakbayram@gmail.com
Genet Couns ; 22(3): 281-5, 2011.
Article in En | MEDLINE | ID: mdl-22029169
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Collection: 01-internacional Database: MEDLINE Main subject: Central Nervous System Diseases / Mutation, Missense / Lymphohistiocytosis, Hemophagocytic / Perforin / Homozygote Type of study: Prognostic_studies Limits: Child / Female / Humans Country/Region as subject: Asia Language: En Journal: Genet Couns Year: 2011 Document type: Article
Search on Google
Print
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Central Nervous System Diseases / Mutation, Missense / Lymphohistiocytosis, Hemophagocytic / Perforin / Homozygote Type of study: Prognostic_studies Limits: Child / Female / Humans Country/Region as subject: Asia Language: En Journal: Genet Couns Year: 2011 Document type: Article