Shorter telomeres in dystrophic muscle consistent with extensive regeneration in young children
- 1 February 2000
- journal article
- research article
- Published by Elsevier BV in Neuromuscular Disorders
- Vol. 10 (2), 113-120
- https://doi.org/10.1016/s0960-8966(99)00093-0
Abstract
No abstract availableKeywords
This publication has 35 references indexed in Scilit:
- Identification of a New Autosomal Dominant Limb-Girdle Muscular Dystrophy Locus on Chromosome 7American Journal of Human Genetics, 1999
- A Gene for Autosomal Recessive Limb-Girdle Muscular Dystrophy in Manitoba Hutterites Maps to Chromosome Region 9q31-q33: Evidence for Another Limb-Girdle Muscular Dystrophy LocusAmerican Journal of Human Genetics, 1998
- Sarcospan, the 25-kDa Transmembrane Component of the Dystrophin-Glycoprotein ComplexPublished by Elsevier BV ,1997
- The Seventh Form of Autosomal Recessive Limb-Girdle Muscular Dystrophy Is Mapped to 17q11-12American Journal of Human Genetics, 1997
- Advances in the molecular genetics of the limb-girdle type of autosomal recessive progressive muscular dystrophyCurrent Opinion in Neurology, 1996
- Mammalian alpha 1- and beta 1-syntrophin bind to the alternative splice-prone region of the dystrophin COOH terminus.The Journal of cell biology, 1995
- Molecular organization at the glycoprotein‐complex‐binding site of dystrophinEuropean Journal of Biochemistry, 1994
- The complete sequence of dystrophin predicts a rod-shaped cytoskeletal proteinCell, 1988
- Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individualsCell, 1987
- ON THE CLASSIFICATION, NATURAL HISTORY AND TREATMENT OF THE MYOPATHIESBrain, 1954