Brain, Vol. 126, No. 9, 2115,
September 2003
© 2003 Guarantors of Brain
doi: 10.1093/brain/awg253
Erratum
Brain, Vol. 126, Part 4, April 2003 (pp. 920–927)A novel nonsense mutation in the ABC1 gene causes a severe syringomyelia-like phenotype of Tangier disease
Stephan Züchner, Anne D. Sperfeld, Jan Senderek, Bernd Sellhaus, Clemens Oliver Hanemann and J. Michael Schröder
The authors wish to point out that the C2665T mutation in the ABC1 gene described in their paper as novel has been previously reported by Marcil et al. (1999):
Marcil M, Brooks-Wilson A, Clee SM, Roomp K, Zhang LH, Yu L, Collins JA, van Dam M, Molhuizen HO, Loubster O, Ouellette BF, Sensen CW, Fichter K, Mott S, Denis M, Boucher B, Pimstone S, Genest J Jr, Kastelein JJ, Hayden MR. Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux. Lancet 1999; 354: 1341–6.
CiteULike 
Connotea 
Del.icio.us What's this?
| ||||||||||||||||||||||||||||||||||||||||||||||||