Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1.

بواسطة Flanigan, K., Gardner, K., Alderson, K., Galster, B., Otterud, B., Leppert, M. F., Kaplan, C., Ptácek, L. J.
منشور في 1996

Automated genomic sequence analysis of the three collagen VI genes: applications to Ullrich congenital muscular dystrophy and Bethlem myopathy

بواسطة Lampe, A, Dunn, D, von Niederhausern, A C, Hamil, C, Aoyagi, A, Laval, S, Marie, S, Chu, M, Swoboda, K, Muntoni, F, Bonnemann, C, Flanigan, K, Bushby, K, Weiss, R
منشور في 2005