Difference of new mutation rates in dystrophic gene between deletion and duplication mutation in Duchenne and Becker muscular dystrophy

Clinical Neurology

Volumn 37, Issue 3, 1997, Pages 212-217

  Kawamura, Jun ^a   Kato, Shingo ^b   Ishihara, Tadayuki ^a   Hiraishi, Yoshiyuki ^b   Kawashiro, Takeo ^a  

^a Higashisaitama National Hospital   (Japan)

^b KEIO UNIVERSITY   (Japan)

Author keywords

Deletion; Duchenne muscular dystrophy; Duplication; Dystrophic; New mutation

Indexed keywords

COMPLEMENTARY DNA; DYSTROPHIN;

ADULT; ARTICLE; BECKER MUSCULAR DYSTROPHY; CONTROLLED STUDY; DUCHENNE MUSCULAR DYSTROPHY; FEMALE; GENE DELETION; GENE DUPLICATION; HETEROZYGOTE; HUMAN; MAJOR CLINICAL STUDY; MUTATION RATE; OOCYTE DEVELOPMENT; SPERMATOGENESIS;

DYSTROPHIN; FEMALE; GENE DELETION; HETEROZYGOTE DETECTION; HUMANS; MALE; MULTIGENE FAMILY; MUSCULAR DYSTROPHIES; OOGENESIS; SPERMATOGENESIS;

EID: 0030794347     PISSN: 0009918X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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