Whole exome sequencing identifies a novel intron heterozygous mutation in TSC2 responsible for tuberous sclerosis complex.

Name: Whole exome sequencing identifies a novel intron heterozygous mutation in TSC2 responsible for tuberous sclerosis complex.
Author: Ye, Yicong

Whole exome sequencing identifies a novel intron heterozygous mutation in TSC2 responsible for tuberous sclerosis complex. — المؤلف: Ye, Yicong — Scientific reports 20201102

المؤلف: Ye, Yicong
النشر: Scientific reports 20201102
الوصف: 4456 p.
الموضوعات: Adult؛ Asian People؛ Codon, Nonsense؛ Computer Simulation؛ Female؛ Heterozygote؛ Humans؛ Introns