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Analysis of ELN gene mutation in a pedigree affected with cutis laxa / 中华医学遗传学杂志
Article in Zh | WPRIM | ID: wpr-776806
Responsible library: WPRO
ABSTRACT
OBJECTIVE@#To carry out genetic diagnosis for a pedigree affected with cutis laxa.@*METHODS@#Genomic DNA was extracted from peripheral blood samples from members of the pedigree and 50 unrelated healthy controls. Potential mutation was screened by next-generation sequencing and verified by Sanger sequencing.@*RESULTS@#A heterozygous c.1985delG mutation was identified in the ELN gene among all patients from this pedigree. The same mutation was not found among unaffected family members and 50 healthy controls.@*CONCLUSION@#The genetic etiology for the pedigree has been elucidated, which has enabled genetic counseling and guidance for reproduction.
Subject(s)
Full text: 1 Database: WPRIM Main subject: Pedigree / Elastin / Cutis Laxa / High-Throughput Nucleotide Sequencing / Genetics / Heterozygote / Mutation Type of study: Guideline Limits: Humans Language: Zh Journal: Zhonghua Yi Xue Yi Chuan Xue Za Zhi Year: 2019 Document type: Article
Full text: 1 Database: WPRIM Main subject: Pedigree / Elastin / Cutis Laxa / High-Throughput Nucleotide Sequencing / Genetics / Heterozygote / Mutation Type of study: Guideline Limits: Humans Language: Zh Journal: Zhonghua Yi Xue Yi Chuan Xue Za Zhi Year: 2019 Document type: Article