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

le Flanigan, K., Gardner, K., Alderson, K., Galster, B., Otterud, B., Leppert, M. F., Kaplan, C., Ptácek, L. J.
Foilsithe 1996

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

le 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
Foilsithe 2005