Analysis of ELN gene mutation in a pedigree affected with cutis laxa / 中华医学遗传学杂志
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; (6): 785-788, 2019.
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.
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