2 results for author:"Jacob R.L." in Literature citations
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| Severe gamma-sarcoglycanopathy caused by a novel missense mutation and a large deletion. Nowak K.J., Walsh P., Jacob R.L., Johnsen R.D., Peverall J., McNally E.M., Wilton S.D., Kakulas B.A., Laing N.G. Neuromuscul. Disord. 10:100-107(2000) · UniProtKB (1) |
| Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy. Nowak K.J., Wattanasirichaigoon D., Goebel H.H., Wilce M., Pelin K., Donner K., Jacob R.L., Hubner C., Oexle K., Anderson J.R. et al. Nat. Genet. 23:208-212(1999) · UniProtKB (1) |