Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals.

Name: Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals.
Author: Kharbanda, Mira

Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals. — المؤلف: Kharbanda, Mira — European journal of medical genetics 20170210

المؤلف: Kharbanda, Mira
النشر: European journal of medical genetics 20170210
الوصف: 130-135 p.
الموضوعات: Adolescent؛ Adult؛ Child؛ Child, Preschool؛ Developmental Disabilities؛ Exome؛ Female؛ Haploinsufficiency