A novel deletion mutation in KMT2A identified in a child with ID/DD and blood eosinophilia.

Name: A novel deletion mutation in KMT2A identified in a child with ID/DD and blood eosinophilia.
Author: Zhang, Haixia

A novel deletion mutation in KMT2A identified in a child with ID/DD and blood eosinophilia. — المؤلف: Zhang, Haixia — BMC medical genetics 20190820

المؤلف: Zhang, Haixia
النشر: BMC medical genetics 20190820
الوصف: 38 p.
الموضوعات: Child؛ Developmental Disabilities؛ Eosinophilia؛ Heterozygote؛ Histone-Lysine N-Methyltransferase؛ Humans؛ Intellectual Disability؛ Loss of Function Mutation