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

Genomics

Volumn 8, Issue 4, 1990, Pages 739-740

  Lavedan, C ^a   Duros, C ^a   Savoy, D ^a   Leblond, S ^b   Bailly, J ^b   Korneluk, R ^b   Junien, C ^a  

^a INSERM   (France)

^b CHILDREN S HOSPITAL OF EASTERN ONTARIO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CREATINE KINASE;

ARTICLE; GENE AMPLIFICATION; HUMAN; MYOTONIC DYSTROPHY; POLYMERASE CHAIN REACTION;

BASE SEQUENCE; BLOTTING, SOUTHERN; CREATINE KINASE; GENETIC MARKERS; HAPLOTYPES; LINKAGE (GENETICS); MOLECULAR SEQUENCE DATA; MYOTONIC DYSTROPHY; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; SUPPORT, NON-U.S. GOV'T;

EID: 0025647219     PISSN: 08887543     EISSN: 10898646     Source Type: Journal    
DOI: 10.1016/0888-7543(90)90265-V     Document Type: Article

References (6)

1. A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19
2. NcoI RFLP at the creatine kinase-muscle type gene locus
3. Molecular diagnosis of myotonic muscular dystrophy by PCR amplification
4. cDNA cloning and mapping of the human creatine kinase M gene to 19q13
5. Isolation and sequence analysis of a fulllength cDNA for human M creatine kinase
6. Rabbit muscle creatine phosphokinase