Molecular bases of dystrophinopathies;Bases moléculaires des dystrophinopathies

Journal de la Societe Biologie

Volumn 199, Issue 1, 2005, Pages 5-11

  Leturcq, France ^a   Kaplan, Jean Claude ^a  

^a Institut Cochin ^*  (France)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 23444431619     PISSN: 12950661     EISSN: None     Source Type: Journal    
DOI: 10.1051/jbio:2005001     Document Type: Conference Paper

References (14)

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6. th ed., 2001, Chap. 19, pp. 385-432.
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11. Monaco A. P., Neve R. L., Colletti-Feener C., Bertelson C. J., Kurnit D. M. & Kunkel L. M., Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene. Nature, 1986, 323, 646-650.
12. Murray J. M., Davies K. E., Harper P. S., Meredith L., Mueller C. R. & Williamson R., Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy. Nature, 1982, 300, 69-71.
13. Nicholson L. V., Johnson M. A., Bushby K. M., Gardner-Medwin D., Curtis A., Ginjaar I. B., den Dunnen J. T., Welch J. L., Butler T. J., Bakker E. & et al., Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 2. Correlations within individual patients. J. Med. Genet., 1993, 30, 737-744.
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