Homozygous NOTCH3 p.R587C mutation in Chinese patients with CADASIL: a case report.

He, Ruojie

Homozygous NOTCH3 p.R587C mutation in Chinese patients with CADASIL: a case report. [electronic resource] - BMC neurology Mar 2020 - 72 p. digital

Publication Type: Case Reports; Journal Article

1471-2377

10.1186/s12883-020-01660-0 doi


Asian People--genetics
Brain--pathology
CADASIL--genetics
Homozygote
Humans
Male
Middle Aged
Mutation
Pedigree
Receptor, Notch3--genetics