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July 11, 2006; 67 (1) Brief Communications

A novel mutation in two families with limb-girdle muscular dystrophy type 2C

D. R. Duncan, P. B. Kang, J. C. Rabbat, C. E. Briggs, H.G.W. Lidov, B. T. Darras, L. M. Kunkel
First published July 10, 2006, DOI: https://doi.org/10.1212/01.wnl.0000223600.78363.dd
D. R. Duncan
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P. B. Kang
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J. C. Rabbat
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C. E. Briggs
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H.G.W. Lidov
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B. T. Darras
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L. M. Kunkel
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Citation
A novel mutation in two families with limb-girdle muscular dystrophy type 2C
D. R. Duncan, P. B. Kang, J. C. Rabbat, C. E. Briggs, H.G.W. Lidov, B. T. Darras, L. M. Kunkel
Neurology Jul 2006, 67 (1) 167-169; DOI: 10.1212/01.wnl.0000223600.78363.dd

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Article Information

vol. 67 no. 1 167-169
DOI: 
https://doi.org/10.1212/01.wnl.0000223600.78363.dd
PubMed: 
16832103

Published By: 
Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology
Print ISSN: 
0028-3878
Online ISSN: 
1526-632X
History: 
  • First Published July 10, 2006.

Copyright & Usage: 
© 2006

Author Disclosures

    1. D. R. Duncan,
    2. P. B. Kang, MD,
    3. J. C. Rabbat, BA,
    4. C. E. Briggs, PhD,
    5. H.G.W. Lidov, MD, PhD,
    6. B. T. Darras, MD and
    7. L. M. Kunkel, PhD
  1. D. R. Duncan,
  2. P. B. Kang, MD,
  3. J. C. Rabbat, BA,
  4. C. E. Briggs, PhD,
  5. H.G.W. Lidov, MD, PhD,
  6. B. T. Darras, MD and
  7. L. M. Kunkel, PhD
  1. From the Program in Genomics, the Howard Hughes Medical Institute (D.R.D., P.B.K., J.C.R., C.E.B., L.M.K.), Department of Neurology (P.B.K., B.T.D.), and Department of Pathology (H.G.W.L.), Children’s Hospital Boston and Harvard Medical School, Boston, MA.
  1. Address correspondence and reprint requests to Dr. Louis M. Kunkel, Division of Genetics, Enders 561, Children’s Hospital Boston, 300 Longwood Avenue, Boston, MA 02115; e-mail: kunkel{at}enders.tch.harvard.edu
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