Identification of mutations in the c-mpl gene in congenital amegakaryocytic thrombocytopenia

Congenital amegakaryocytic thrombocytopenia (CAMT) is a rare disorder expressed in infancy and characterized by isolated thrombocytopenia and megakaryocytopenia with no physical anomalies. Our previous hematological analysis indicated similarities between human CAMT and murine c-mpl (thrombopoietin...

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Bibliographic Details
Main Authors: Ihara, Kenji, Ishii, Eiichi, Eguchi, Mariko, Takada, Hidetoshi, Suminoe, Aiko, Good, Robert A., Hara, Toshiro
Format: Artigo
Language:Inglês
Published: The National Academy of Sciences 1999
Subjects:
Biological Sciences
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC15907/
https://ncbi.nlm.nih.gov/pubmed/10077649
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