Article
BRAT1-associated neurodegeneration: Intra-familial phenotypic differences in siblings.
American journal of medical genetics. Part A - 1 Nov 2016
Smith Nicholas J, Lipsett Jill, Dibbens Leanne M, Heron Sarah E
Abstract excerpt
Recessive mutations in BRAT1 cause lethal neonatal rigidity and multifocal seizure syndrome, a phenotype characterized by neonatal microcephaly, hypertonia, and refractory epilepsy with premature death by age 2 years. Recently, attenuated disease variants have been described, suggesting that a wider clinical spectrum of BRAT1-associated neurodegeneration exists than was previously thought. Here, we report two...
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