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One base deletion in the cysteine-rich domain of the dystrophin gene in Duchenne musculas dystrophy patients

Author
TSUKAMOTO, H; INUI, K; MATSUOKA, T; YANAGIHARA, I; FUKUSHIMA, H; OKADA, S
Osaka univ., fac. medicine, dep. pediatrics, Suita Osaka 565, Japan
Source

Human molecular genetics (Print). 1994, Vol 3, Num 6, pp 995-996 ; ref : 22 ref

ISSN
0964-6906
Scientific domain
Genetics
Publisher
Oxford University Press, Oxford
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Dystrophie musculaire progressive Duchenne Dystrophine Délétion Gène Génétique Homme Mutation Maladie héréditaire Neuromusculaire pathologie Système nerveux pathologie
Keyword (en)
Duchenne muscular dystrophy Dystrophin Deletion Gene Genetics Human Mutation Genetic disease Neuromuscular diseases Nervous system diseases
Keyword (es)
Distrofia muscular progresiva Duchenne Distrofina Deleción Gen Genética Hombre Mutación Enfermedad hereditaria Neuromuscular patología Sistema nervioso patología
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17H Diseases of striated muscles. Neuromuscular diseases

Discipline
Neurology
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
4126378

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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