论文信息 - Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity. - 字舞流文

Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity.

P. Lantos | S. Mead | J. Collinge | S. Joiner | J. Linehan | J. Wadsworth | J. Beck | A. King | T. Campbell | M. Poulter | J. D. Wadsworth | T. Webb | M. Desbruslais | Susan Joiner | Melanie Desbruslais