Literature DB >> 1355071

A novel NcoI polymorphism creates a fifth haplotype in the 3' untranslated region of CKM.

A M Differ1, M Bobrow, C G Mathew.   

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.

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Year:  1992        PMID: 1355071     DOI: 10.1007/bf00221966

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  1 in total

1.  Direct haplotyping by double digestion of PCR-amplified creatine kinase (CKMM): application to myotonic dystrophy diagnosis.

Authors:  C Lavedan; C Duros; D Savoy; S Leblond; J Bailly; R Korneluk; C Junien
Journal:  Genomics       Date:  1990-12       Impact factor: 5.736

  1 in total

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