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

Por Flanigan, K., Gardner, K., Alderson, K., Galster, B., Otterud, B., Leppert, M. F., Kaplan, C., Ptácek, L. J.
Publicado em 1996

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

Por 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
Publicado em 2005