[Identification of the dystrophin gene deletions in DMD/BMD patients. Analysis of the reading frame shift and germinal mosaicism]
Minerva Pediatr
.
1991 Mar;43(3):65-6.
[Article in Italian]
Authors
A E Covone
1
,
F Caroli
,
A Cereseto
,
M Lerone
,
G Romeo
Affiliation
1
Laboratorio di Genetica Molecolare, Istituto G. Gaslini, Genova.
PMID:
1870527
No abstract available
MeSH terms
Child
Chromosome Deletion*
DNA / genetics
Dystrophin / genetics*
Humans
Mosaicism / genetics*
Muscular Dystrophies / genetics*
Reading Frames / genetics*
Substances
Dystrophin
DNA