doi: 10.1007/BF00221966.
A novel NcoI polymorphism creates a fifth haplotype in the 3' untranslated region of CKM
Affiliations
- PMID: 1355071
- DOI: 10.1007/BF00221966
Item in Clipboard
A novel NcoI polymorphism creates a fifth haplotype in the 3' untranslated region of CKM
Hum Genet.
1992 Aug.
Abstract
A novel NcoI polymorphism has been detected in the 3' untranslated region of the creatinine kinase (CKM) gene. The addition NcoI restriction site creates a fifth haplotype for the NcoI and TaqI restriction fragments length polymorphisms at this locus, and segregates with the myotonic dystrophy gene in 3 generations of an affected family.
Similar articles
-
3' creatine kinase (M-type) polymorphisms linked to myotonic dystrophy in Italian and Spanish populations.Hum Genet. 1991 Oct;87(6):654-6. doi: 10.1007/BF00201719. Hum Genet. 1991. PMID: 1682233
-
NcoI and TaqI RFLPs for human M creatine kinase (CKM).Nucleic Acids Res. 1988 Sep 12;16(17):8744. doi: 10.1093/nar/16.17.8744. Nucleic Acids Res. 1988. PMID: 2901731 Free PMC article. No abstract available.
-
Physical and genetic mapping of a novel chromosome 19 ERCC1 marker showing close linkage with myotonic dystrophy.Genomics. 1991 Mar;9(3):500-4. doi: 10.1016/0888-7543(91)90416-c. Genomics. 1991. PMID: 1674498
-
NcoI RFLP in human brain creatine kinase gene (CKBB).Nucleic Acids Res. 1991 Jan 11;19(1):195. doi: 10.1093/nar/19.1.195-a. Nucleic Acids Res. 1991. PMID: 1672741 Free PMC article.
-
[Myotonic dystrophy of Steinert].J Genet Hum. 1989 Jan;37(1):51-4. J Genet Hum. 1989. PMID: 2565953 Review. French.
References
-
- Genomics. 1990 Dec;8(4):739-40 - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources
Miscellaneous