Point mutations and polymorphisms in the human dystrophin gene identified in genomic DNA sequences amplified by multiplex PCR
- Author
- KILIMANN, M. W1 ; PIZZUTI, A1 ; GROMPE, M1 ; THOMAS CASKEY, C1
[1] Baylor coll. medicine, inst. molecular genetics, Houston TX 77030, United States - Source
Human genetics. 1992, Vol 89, Num 3, pp 253-258 ; ref : 1/2 p
- CODEN
- HUGEDQ
- ISSN
- 0340-6717
- Scientific domain
- Biotechnology; Genetics
- Publisher
- Springer, Berlin
/
Springer, Heidelberg
/
Springer, New York, NY
- Publication country
- Germany
- Document type
- Article
- Language
- English
- Keyword (fr)
- Dystrophie musculaire progressive Duchenne Dystrophine Gène Homme Mutation ponctuelle Pathogénie Polymorphisme Système nerveux pathologie
- Keyword (en)
- Duchenne muscular dystrophy Dystrophin Gene Human Point mutation Pathogenesis Polymorphism Nervous system diseases
- Keyword (es)
- Distrofia muscular progresiva Duchenne Distrofina Gen Hombre Mutación puntual Patogenia Polimorfismo Sistema nervioso patología
- Classification
- Discipline
- Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4355463
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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DOI
10.1007/BF00220535 
https://dx.doi.org/10.1007/BF00220535
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