Preservation of the C-terminus of dystrophin molecule in the skeletal muscle from Becker muscular dystrophy
Kiichi Arahata, Louis M. Kunkel(Howard Hughes Medical Institute), Chikahiko Eguchi(Ajinomoto (Japan)), Hideo Sugita, Eri Arikawa(National Center of Neurology and Psychiatry), Misako Kaido(National Center of Neurology and Psychiatry), Alan H. Beggs(Broad Institute), Hideo Honda(Fujirebio (Japan)), Satoru Ito(Fujirebio (Japan)), Satoshi Orimo(Japan Atomic Energy Agency), Ikuya Nonaka, Shoichi Ishiura(Niigata University of Health and Welfare), Tsuneo Ishiguro(Ajinomoto (Japan)), Toshifumi Tsukahara(Japan Advanced Institute of Science and Technology)
Cited by 91
Related Papers
Genotype-Phenotype Correlation in the Long-QT Syndrome
|Circulation|2001|1.8k
Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis
|Nature Genetics|2000|1.3k
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.
|PubMed|1989|961
Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)
|Nature|2000|941
ACTN3 Genotype Is Associated with Human Elite Athletic Performance
|The American Journal of Human Genetics|2003|917