A novel mutation in the MECOM gene causing radioulnar synostosis with amegakaryocytic thrombocytopenia (RUSAT‐2) in an infant
Autor: | Thangadorai Ravikumar, Deenadayalan Munirathnam, Ajeitha Loganathan |
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Rok vydání: | 2018 |
Předmět: |
business.industry
Hematology Amegakaryocytic thrombocytopenia Bioinformatics 03 medical and health sciences 0302 clinical medicine MECOM gene Oncology 030220 oncology & carcinogenesis Pediatrics Perinatology and Child Health Mutation (genetic algorithm) Radioulnar synostosis Medicine business Novel mutation 030215 immunology |
Zdroj: | Pediatric Blood & Cancer. :e27574 |
ISSN: | 1545-5017 1545-5009 |
Databáze: | OpenAIRE |
Externí odkaz: |