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A novel mutation in the MECOM gene causing radioulnar synostosis with amegakaryocytic thrombocytopenia (RUSAT‐2) in an infant
Author(s) -
Loganathan Ajeitha,
Munirathnam Deenadayalan,
Ravikumar Thangadorai
Publication year - 2019
Publication title -
pediatric blood and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.116
H-Index - 105
eISSN - 1545-5017
pISSN - 1545-5009
DOI - 10.1002/pbc.27574
Subject(s) - tamil , medicine , hematology , family medicine , pediatrics , philosophy , linguistics
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