New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome.
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K. Ohno | S. Sine | C. Bouzat | M. Milone | J. Pruitt | A. Engel | S. Nakano | J. Brengman | N. Bren | J. Sieb | D. Hutchinson | H. L. Wang | H. L. Wang | Kinji Ohno | Cecilia Bouzat | A. G. Engel | Satoshi Nakano | Joern P. Sieb