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Biochemical and Biophysical Research Communications

Volumn 238, Issue 2, 1997, Pages 492-497

Targeted disruption of exon 52 in the mouse dystrophin gene induced muscle degeneration similar to that observed in duchenne muscular dystrophy

(8) Araki, Eiichi a Nakamura, Kenji b Nakao, Kazuki b Kameya, Shuhei c Kobayashi, Osamu c Nonaka, Ikuya c Kobayashi, Takuro a Katsuki, Motoya b

a KYUSHU UNIVERSITY (Japan)

b UNIVERSITY OF TOKYO (Japan)

c NATIONAL INSTITUTE OF NEUROSCIENCE (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

DYSTROPHIN; ISOPROTEIN; MUTANT PROTEIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; DELETION MUTANT; DUCHENNE MUSCULAR DYSTROPHY; EXON; GENE DISRUPTION; GENE MUTATION; MOUSE; MUSCLE ATROPHY; MUSCLE CELL; MUSCLE HYPERTROPHY; MUSCLE NECROSIS; MUSCLE REGENERATION; NONHUMAN; PRIORITY JOURNAL;

EID: 0031577559 PISSN: 0006291X EISSN: None Source Type: Journal
DOI: 10.1006/bbrc.1997.7328 Document Type: Article

Times cited : (111)

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