Sewry, C. A.
Great Ormond Street Hospital
3 papers on CoChatORCID 0000-0003-4870-582X
Most cited papers
- Verified
Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan
Godfrey, C., Clement, E., Mein, R., Brockington, M., Smith, J., Talim, B., Straub, V., Robb, S., Quinlivan, R., Feng, L., et al. (2007) · Brain
Muscle Physiology and DisordersGlycosylation and Glycoproteins Research
Cited by 441
- Verified
Mutation in BAG3 causes severe dominant childhood muscular dystrophy
Selcen, D., Muntoni, F., Burton, B. K., Pegoraro, E., Sewry, C., Bite, A. V., & Engel, A. G. (2009) · Annals of Neurology
Muscle Physiology and DisordersCardiomyopathy and Myosin Studies
Cited by 357
- Verified
Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination as an Alternate Pathway to Myofibrillar Disruption in Nemaline Myopathy
Gupta, V. A., Ravenscroft, G., Shaheen, R., Todd, E. J., Swanson, L. C., Shiina, M., Ogata, K., Hsu, C., Clarke, N. F., Darras, B. T., et al. (2013) · The American Journal of Human Genetics
Muscle Physiology and DisordersGenomics and Rare Diseases
Cited by 168
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