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Somatic Cell and Molecular Genetics|November 1, 1987
Regional localization of the murine Duchenne muscular dystrophy gene on the mouse X chromosomeJ S Chamberlain, S G Grant, A A Reeves, et al.Neurology|June 13, 2001
MeCP2 mutations in children with and without the phenotype of Rett syndromeK Hoffbuhr, J M Devaney, B LaFleur, et al.Human Molecular Genetics|May 23, 1998
Caveolin-3 in muscular dystrophyE M McNally, E de Sá Moreira, D J Duggan, et al.Human Molecular Genetics|November 1, 1996
Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophyE M McNally, D Duggan, J R Gorospe, et al.Neurology|May 30, 2002
Molecular findings in symptomatic and pre-symptomatic Alexander disease patientsJ R Gorospe, S Naidu, A B Johnson, et al.Neurology|December 24, 2010
SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophyE Pegoraro, E P Hoffman, L Piva, et al.Nature Genetics|May 20, 1998
Mutations in the integrin alpha7 gene cause congenital myopathyY K Hayashi, F L Chou, E Engvall, et al.Neurology|April 1, 1995
Genetic and biochemical normalization in female carriers of Duchenne muscular dystrophy: evidence for failure of dystrophin production in dystrophin-competent myonucleiE Pegoraro, R N Schimke, C Garcia, et al.International Journal of Obesity (2005)|December 9, 2010
Adiposity attenuates muscle quality and the adaptive response to resistance exercise in non-obese, healthy adultsM D Peterson, D Liu, H Gordish-Dressman, et al.Gene|September 15, 2012
Leptin and leptin receptor genetic variants associate with habitual physical activity and the arm body composition response to resistance trainingS Walsh, C J Haddad, M A Kostek, et al.Pageof 19