Ausgabe 4/2000
Inhalt (7 Artikel)
Tau gene mutations in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)
M. G. Spillantini, J.C. Van Swieten, M. Goedert
Parkinson disease: analysis of mitochondrial DNA in monozygotic twins
S. Kösel, E. M. Grasbon-Frodl, J. M. Hagenah, M. B. Graeber, P. Vieregge
The murine Bis1 seizure gene and the Kcnab2 gene encoding the β2-subunit of the K+ channel are different
P. Zerr, B. Martin, J. P. Adelman
SCA2 alleles are not general predisposition factors for multiple sclerosis
B. Miterski, J. T. Epplen, D. Poehlau, E. Sindern, M. Haupts
Aceruloplasminemia with a novel mutation associated with parkinsonism
S. Kohno, H. Miyajima, Y. Takahashi, Y. Inoue
Genetic studies in autistic disorder and chromosome 15
M. P. Bass, M. M. Menold, C. M. Wolpert, S. L. Donnelly, S. A. Ravan, E. R. Hauser, L. O. Maddox, J. M. Vance, R. K. Abramson, H. H. Wright, J. R. Gilbert, M. L. Cuccaro, G. R. DeLong, M. A. Pericak-Vance
Progress in the clinical and molecular genetics of familial parkinsonism
T. Kitada, S. Asakawa, H. Matsumine, N. Hattori, H. Shimura, S. Minoshima, N. Shimizu, Y. Mizuno