Transient JAK2 V617F mutation in an aplastic anaemia patient with a paroxysmal nocturnal haemoglobinuria clone. | Br J Haematol;161(2): 297-8, 2013 Apr. | MEDLINE

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Transient JAK2 V617F mutation in an aplastic anaemia patient with a paroxysmal nocturnal haemoglobinuria clone.

Langabeer, Stephen E; Haslam, Karl; O'Brien, David; Enright, Helen; Leahy, Maeve.

Br J Haematol ; 161(2): 297-8, 2013 Apr.

Article in En | MEDLINE | ID: mdl-23360357

Subject(s)

Anemia, Aplastic/genetics; Hemoglobinuria, Paroxysmal/genetics; Janus Kinase 2/genetics; Mutation, Missense; Amino Acid Substitution; Anemia, Aplastic/complications; Female; Hemoglobinuria, Paroxysmal/complications; Humans; Male

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mutation, Missense / Janus Kinase 2 / Hemoglobinuria, Paroxysmal / Anemia, Aplastic Limits: Female / Humans / Male Language: En Journal: Br J Haematol Year: 2013 Document type: Article

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Mutation, Missense / Janus Kinase 2 / Hemoglobinuria, Paroxysmal / Anemia, Aplastic Limits: Female / Humans / Male Language: En Journal: Br J Haematol Year: 2013 Document type: Article