Ausgabe 3/1998
Inhalt (10 Artikel)
No genetic association between the LRP receptor and sporadic or late-onset familial Alzheimer disease
William K. Scott, Larry H. Yamaoka, Meredyth P. Bass, P. Craig Gaskell, P. Michael Conneally, Gary W. Small, Lindsay A. Farrer, Sanford A. Auerbach, Ann M. Saunders, Allen D. Roses, J. L. Haines, Margaret A. Pericak-Vance
Clinical and molecular genetics of primary dystonias
U. Müller, Daniela Steinberger, Andrea H. Németh
Genetic fine mapping of the Miyoshi myopathy locus and exclusion of eight candidate genes
K. Bejaoui, J. Liu, D. McKenna-Yasek, D. Le Paslier, K. Bossie, D. M. Gilligan, R. H. Brown
Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease
Siegfried Kösel, E. M. Grasbon-Frodl, Ulrike Mautsch, Rupert Egensperger, U. von Eitzen, Dimitrij Frishman, Sabine Hofmann, Klaus-Dieter Gerbitz, Parviz Mehraein, Manuel B. Graeber
Identification of two mutations and a polymorphism in the chloride channel CLCN-1 in patients with Becker's generalized myotonia
Jesus Esteban, A. M. Neumeyer, Diane McKenna-Yasek, R. H. Brown
Adult-onset glycogen storage disease type II: phenotypic and allelic heterogeneity in German patients
M. Vorgerd, Barbara Burwinkel, Heinz Reichmann, Jean-Pierre Malin, Manfred W. Kilimann
Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosis
Teepu Siddique, M. A. Pericak-Vance, Janice Caliendo, Seong-Tshool Hong, W.-Y. Hung, Jocelyn Kaplan, Diane McKenna-Yasek, Jackie B. Rimmler, Peter Sapp, Ann M. Saunders, William K. Scott, Nailah Siddique, J. L. Haines, Robert H. Brown
Histopathology and APOE genotype of the first Alzheimer disease patient, Auguste D.
M. B. Graeber, S. Kösel, E. Grasbon-Frodl, H. J. Möller, P. Mehraein
Chromosomal localization of two genes underlying late-infantile neuronal ceroid lipofuscinosis
J. L. Haines, Rose-Mary N. Boustany, Joseph Alroy, Kristen J. Auger, Kerida S. Shook, Henry Terwedow, T. J. Lerner