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Hall TE, Wood AJ, Ehrlich O, et al. (2019) Cellular rescue in a zebrafish model of congenital muscular dystrophy type 1A. Npj Regenerative Medicine. 4: 21 |
Sztal T, Zhao M, Currie P, et al. (2013) P.9.12 Exploring the pathological mechanism of Actin myopathies in zebrafish Neuromuscular Disorders. 23: 787 |
Currie PD, Schilling TF, Ingham PW. (2008) Small-scale marker-based screening for mutations in zebrafish development. Methods in Molecular Biology (Clifton, N.J.). 461: 493-512 |
Svetic V, Hollway GE, Elworthy S, et al. (2007) Sdf1a patterns zebrafish melanophores and links the somite and melanophore pattern defects in choker mutants. Development (Cambridge, England). 134: 1011-22 |