Literature DB >> 2901731

NcoI and TaqI RFLPs for human M creatine kinase (CKM)

M B Perryman1, J F Hejtmancik, T Ashizawa, R Armstrong, S C Lin, R Roberts, H F Epstein.   

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Year:  1988        PMID： 2901731      PMCID： PMC338622          DOI： 10.1093/nar/16.17.8744

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  1 in total

1.  Isolation and sequence analysis of a full-length cDNA for human M creatine kinase.

Authors:  M B Perryman; S A Kerner; T J Bohlmeyer; R Roberts
Journal:  Biochem Biophys Res Commun       Date:  1986-11-14       Impact factor: 3.575
  1 in total
  6 in total

1.  Male neonatal death and progressive weakness and immune deficiency in females: an unknown X linked condition.

Authors:  G Woods; G Black; G Norbury
Journal:  J Med Genet       Date:  1995-03       Impact factor: 6.318

2.  Assessment of a creatine kinase isoform M defect as a cause of myotonic dystrophy and the characterization of two novel CKMM polymorphisms.

Authors:  J Bailly; A E MacKenzie; S Leblond; R G Korneluk
Journal:  Hum Genet       Date:  1991-03       Impact factor: 4.132

3.  Linkage disequilibrium detected between myotonic dystrophy and the anonymous marker D19S63 in the Spanish population.

Authors:  A Cobo; D Grinberg; S Balcells; L Vilageliu; R Gonzàlez-Duarte; M Baiget
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

4.  A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus.

Authors:  K Johnson; P Shelbourne; J Davies; J Buxton; E Nimmo; M J Siciliano; L L Bachinski; M Anvret; H Harley; S Rundle
Journal:  Am J Hum Genet       Date:  1990-06       Impact factor: 11.025

5.  Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish population.

Authors:  P Nokelainen; L Alanen-Kurki; R Winqvist; B Falck; H Somer; J Leisti; K Johnson; M L Savontaus; L Peltonen
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

6.  Negative expansion of the myotonic dystrophy unstable sequence.

Authors:  D Abeliovich; I Lerer; I Pashut-Lavon; E Shmueli; A Raas-Rothschild; M Frydman
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025
  6 in total

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