TY  - GEN
AU  - Lesca,G
AU  - Demarquay,G
AU  - Llense,S
AU  - Streichenberger,N
AU  - Petiot,P
AU  - Michel-Calemard,L
AU  - Récan,D
AU  - Vial,C
AU  - Ollagnon-Roman,E
TI  - [Symptomatic carriers of dystrophinopathy with chromosome X inactivation bias]
SN  - 0035-3787
PY  - 2003///1201
KW  - Adolescent
KW  - Adult
KW  - Chromosomes, Human, X
KW  - genetics
KW  - Codon, Terminator
KW  - Dystrophin
KW  - Exons
KW  - Family
KW  - Female
KW  - Gene Silencing
KW  - Heterozygote
KW  - Humans
KW  - Immunohistochemistry
KW  - Male
KW  - Middle Aged
KW  - Muscle Weakness
KW  - etiology
KW  - Muscle, Skeletal
KW  - pathology
KW  - Muscular Dystrophies
KW  - Muscular Dystrophy, Duchenne
KW  - Pedigree
N1  - Publication Type: Case Reports; English Abstract; Journal Article
ER  -