Back to Search
Start Over
A NOVEL MISSENSE MUTATION IN THE DKC1 GENE IN A JAPANESE FAMILY WITH X-LINKED DYSKERATOSIS CONGENITA
- Source :
- Pediatric Hematology and Oncology. 19:413-419
- Publication Year :
- 2002
- Publisher :
- Informa UK Limited, 2002.
-
Abstract
- The authors report 2 male patients with dyskeratosis congenita (DC) in a Japanese kindred. Sequencing of the complementary DNA of the dyskerin gene (DKC1) revealed a T-to-C transition at nucleotide 1285 in exon 12 that resulted in a novel missense mutation L398P. Despite harboring the same mutation in the DKC1 gene, one patient had significantly milder hematological symptoms than the other, indicating that there may be other factors that determine the severity of DC.
- Subjects :
- Male
DNA, Complementary
Genetic Linkage
Mutation, Missense
Cell Cycle Proteins
Biology
medicine.disease_cause
Dyskeratosis Congenita
Dyskerin
Exon
Complementary DNA
medicine
Humans
Missense mutation
Child
Gene
Genetics
Chromosomes, Human, X
Mutation
Transition (genetics)
Nuclear Proteins
Hematology
medicine.disease
Oncology
Pediatrics, Perinatology and Child Health
Polymorphism, Restriction Fragment Length
Dyskeratosis congenita
Subjects
Details
- ISSN :
- 15210669 and 08880018
- Volume :
- 19
- Database :
- OpenAIRE
- Journal :
- Pediatric Hematology and Oncology
- Accession number :
- edsair.doi.dedup.....42f75ed1d701b3992b66f8799f7cf204
- Full Text :
- https://doi.org/10.1080/08880010290097170