Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy.
about
A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies.Dystrophin gene mutation location and the risk of cognitive impairment in Duchenne muscular dystrophyDystrophin expression in muscle stem cells regulates their polarity and asymmetric division.Neuronal SH-SY5Y cells use the C-dystrophin promoter coupled with exon 78 skipping and display multiple patterns of alternative splicing including two intronic insertion events.The lived experience of hope among parents of a child with Duchenne muscular dystrophy: perceiving the human being beyond the illness.Molecular characterization of co-occurring Duchenne muscular dystrophy and X-linked oculo-facio-cardio-dental syndrome in a girl.
P2860
Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy.
description
2004 nî lūn-bûn
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name
Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy.
@en
Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy.
@nl
type
label
Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy.
@en
Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy.
@nl
prefLabel
Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy.
@en
Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy.
@nl
P2093
P2860
P1476
Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy.
@en
P2093
Florencia Giliberto
Irene Szijan
Verónica Ferreiro
Viviana Dalamon
P2860
P356
10.1179/016164104773026589
P577
2004-01-01T00:00:00Z