Ausgabe 1/2000
Inhalt (10 Artikel)
A gene for autosomal dominant juvenile amyotrophic lateral sclerosis (ALS4 ) localizes to a 500-kb interval on chromosome 9q34
I. P. Blair, C. L. Bennett, A. Abel, B. A. Rabin, J. W. Griffin, K. H. Fischbeck, D. R. Cornblath, P. F. Chance
CLN -encoded proteins do not interact with each other
N. A. Zhong, D. N. Moroziewicz, W. Ju, K. E. Wisniewski, A. Jurkiewicz, W. T. Brown
Evidence for allelic association of the dopamine β-hydroxylase gene (DBH) with susceptibility to typical migraine
R. A. Lea, A. Dohy, K. Jordan, S. Quinlan, P. J. Brimage, L. R. Griffiths
Mutation analysis of the hCHK2 gene in primary human malignant gliomas
D. N. Louis, Y. Ino, D. C. R. Wahrer, D. W. Bell, D. A. Haber
Sequence analysis of the MTCYB gene in Parkinson disease
U. von Eitzen, S. Kösel, E. M. Grasbon-Frodl, R. Egensperger, M. B. Graeber
Charcot-Marie-Tooth disease and related peripheral neuropathies: novel mutations in the peripheral myelin genes connexin 32 (Cx32 ), peripheral myelin protein 22 (PMP22 ), and peripheral myelin protein zero (MPZ )
A. B. Ekici, D. Schweitzer, O. Park, D. Lorek, B. Rautenstrauss, G. Krüger, W. Friedl, S. Uhlhaas, K. Bathke, D. Heuss, C. Kayser, H. Grehl
The parental origin of new mutations in neurofibromatosis 2
L. Kluwe, V. Mautner, D. M. Parry, L. B. Jacoby, M. Baser, J. Gusella, K. Davis, D. Stavrou, M. MacCollin
The survival motor neuron (SMN) protein: effect of exon loss and mutation on protein localization
T. T. Le, D. D. Coovert, U. R. Monani, G. E. Morris, A. H. M. Burghes
Supporting evidence of a gene for partial epilepsy on 10q
V.-F. Mautner, M. Lindenau, A. Gottesleben, G. Goetze, L. Kluwe
Developmental profile of Sry transcripts in mouse brain
A. Mayer, G. Mosler, W. Just, C. Pilgrim, I. Reisert