Current Concepts in Dystrophinopathies
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s12098-014-1621-2.pdf
Reference34 articles.
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2. Monaco AP, Nerve RL, Colletti-Feener C, Bertelson CJ, Kurnit DM, Kunkel LM. Isolation of candidate cDNA’s for portions of the Duchenne muscular dystrophy gene. Nature. 1986;323:646–50.
3. Koenig M, Hoffman EP, Berteleson CJ, Monaco AP, Feener C, Kunkel LM. Complete cloning of the Duchenne muscular dystrophy cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell. 1987;50:509–17.
4. Koenig M, Monaco AP, Kunkel LM. The complete sequence of the dystrophin predicts a rod shaped cyto-skeleton protein. Cell. 1988;53:219–26.
5. Hoffman EP, Brown Jr RH, Kunkel LM. Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell. 1987;51:919–28.
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1. Duchenne Muscular Dystrophy: A Practice Update;The Indian Journal of Pediatrics;2017-06-27
2. Modulation of Myotilin and Fylamin C in Various Muscle Diseases: A Microarray Analysis;Journal of Functional Morphology and Kinesiology;2016-02-19
3. Editorial: Advances in Neurology;The Indian Journal of Pediatrics;2015-01-24
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