Ausgabe 1/1997
Inhalt (11 Artikel)
Multiple sclerosis: a polygenic disease involving epistatic interactions, germline rearrangements and environmental effects
Marcela V. Karpuj, Lawrence Steinman, Jorge R. Oksenberg
A possible role of NAIP gene deletions in sex-related spinal muscular atrophy phenotype variation
Giuseppe Novelli, Sabrina Semprini, Francesca Capon, Bruno Dallapiccola
ANOVA, a putative astrocytic RNA-binding protein gene that maps to chromosome 19q13.3
Keisuke Ueki, Shivapriya Ramaswamy, Stephanie J. Billings, Harvey W. Mohrenweiser, David N. Louis
The genomic organization of human dystrobrevin
Hélène M. Sadoulet-Puccio, Chris A. Feener, Daniel J. Schaid, Stephen N. Thibodeau, Virginia V. Michels, Louis M. Kunkel
Locus heterogeneity in Friedreich ataxia
Markus Kostrzewa, Thomas Klockgether, Maxwell S. Damian, Ulrich Müller
Mutations in the δ-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2)
David J. Duggan, David Manchester, Karen P. Stears, Dennis J. Mathews, Carolyn Hart, Eric P. Hoffman
SCA2 trinucleotide expansion in German SCA patients
Olaf Riess, Franco A. Laccone, Suzana Gispert, Ludger Schöls, Christine Zühlke, Ana Maria Menezes Vieira-Saecker, Susanne Herlt, Karl Wessel, Jörg T. Epplen, Bernhard H.F. Weber, Friedmar Kreuz, Soheyla Chahrokh-Zadeh, Alfons Meindl, Astrid Lunkes, Jorge Aguiar, Milan Macek Jr, Alice Krebsová, Milan Macek Sen, Katrin Bürk, Sigrid Tinschert, Isolde Schreyer, Stefan-M. Pulst, Georg Auburger
Exon 5 encoded domain is not required for the toxic function of mutant SOD1 but essential for the dismutase activity: identification and characterization of two new SOD1 mutations associated with familial amyotrophic lateral sclerosis
James S. Zu, Han-Xiang Deng, Terence P. Lo, Hiroshi Mitsumoto, Mohamed S. Ahmed, Wu-Yen Hung, Zi-Jian Cai, John A. Tainer, Teepu Siddique
Rediscovery of the case described by Alois Alzheimer in 1911: historical, histological and molecular genetic analysis
M.B. Graeber, S. Kösel, R. Egensperger, R.B. Banati, U. Müller, K. Bise, P. Hoff, H.J. Möller, K. Fujisawa, P. Mehraein