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pro vyhledávání: '"K. Priya Karthikeyan"'
Autor:
V. Manjunath, S. G. Thenral, B. R. Lakshmi, Atchayaram Nalini, A. Bassi, K. Priya Karthikeyan, K. Piyusha, R. Menon, A. Malhotra, L. S. Praveena, R. M. Anjanappa, S. M. Sakthivel Murugan, Kiran Polavarapu, Mainak Bardhan, V. Preethish-Kumar, Seena Vengalil, Saraswati Nashi, S. Sanga, M. Acharya, R. Raju, V. R. Pai, V. L. Ramprasad, R. Gupta
Publikováno v:
Human Mutation. 2023:1-10
The sarcoglycanopathies are autosomal recessive limb-girdle muscular dystrophies (LGMDs) caused by the mutations in genes encoding the α, β, γ, and δ proteins which stabilizes the sarcolemma of muscle cells. The clinical phenotype is characterize