Mutation analysis of a pedigree affected with brachydactyly type E2 and obesity / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
; (6): 257-259, 2019.
Article
ي Zh
| WPRIM
| ID: wpr-772030
المكتبة المسؤولة:
WPRO
ABSTRACT
OBJECTIVE@#To identify pathogenic mutation in a pedigree affected with brachydactyly and obesity.@*METHODS@#Peripheral blood sample was collected for extraction of genomic DNA. Exons capture combined with next generation sequencing (NGS) was carried out to identify potential mutation. Sanger sequencing was used to verify the results.@*RESULTS@#NGS has identified a novel heterozygous missense mutation (c.125A>C, p.Gln42Pro) in the exon 1 of PTHLH gene. The result was verified by Sanger sequencing. The mutations was derived from his mother. His uncle and sister have also carried the same heterozygous mutation.@*CONCLUSION@#A novel mutation of the PTHLH gene has been identified in a pedigree affected with brachydactyly type E2 and obesity.
النص الكامل:
1
الفهرس:
WPRIM
الموضوع الرئيسي:
Pedigree
/
DNA Mutational Analysis
/
Brachydactyly
/
Mutation
/
Obesity
المحددات:
Humans
اللغة:
Zh
مجلة:
Chinese Journal of Medical Genetics
السنة:
2019
نوع:
Article