Impairment of capping in lymphoblastoid cell lines of Duchenne patients indicates an intrinsic cellular defect
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00285158.pdf
Reference13 articles.
1. Burghes AH, Logan C, Hu X, Belfall B, Worton RG, Ray PN (1987) A cDNA clone from the Duchenne/Becker muscular dystrophy gene. Nature 328:434?437
2. Chelly J, Kaplan JC, Maire P, Gautron S, Kahn A (1988) Transcription of the dystrophin gene in human muscle and non-muscle tissues. Nature 333:858?860
3. Goldsmith BM, Greumer HD (1987) Systemic membrane defect and the inhibition of lymphocyte capping in Duchenne muscular dystrophy. Clin Chim Acta 164:33?46
4. Hoffman EP, Brown HR, Kunkel LM (1987a) Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell 51:919?928
5. Hoffman EP, Knudson CM, Campbell KD, Kunkel LM (1987b) Subcellular fractionation of dystrophin to the triads of skeletal muscle. Nature 330:754?758
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