Ausgabe 3/2009
Inhalt (11 Artikel)
Whole-genome conditional two-locus analysis identifies novel candidate genes for late-onset Parkinson’s disease
A. González-Pérez, J. Gayán, J. Marín, J. J. Galán, M. E. Sáez, L. M. Real, C. Antúnez, A. Ruiz
Extended tracts of homozygosity identify novel candidate genes associated with late-onset Alzheimer’s disease
M. A. Nalls, R. J. Guerreiro, J. Simon-Sanchez, J. T. Bras, B. J. Traynor, J. R. Gibbs, L. Launer, J. Hardy, A. B. Singleton
Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindred
Ester Cuenca-León, Roser Corominas, Magda Montfort, Josep Artigas, Manuel Roig, Mònica Bayés, Bru Cormand, Alfons Macaya
Association between migraine and a functional polymorphism at the dopamine β-hydroxylase locus
F. Fernandez, N. Colson, S. Quinlan, J. MacMillan, R. A. Lea, L. R. Griffiths
Examination of association of genes in the serotonin system to autism
B. M. Anderson, N. C. Schnetz-Boutaud, J. Bartlett, A. M. Wotawa, H. H. Wright, R. K. Abramson, M. L. Cuccaro, J. R. Gilbert, M. A. Pericak-Vance, J. L. Haines
Interaction of the SPG21 protein ACP33/maspardin with the aldehyde dehydrogenase ALDH16A1
Michael C. Hanna, Craig Blackstone
Molecular analysis of NPC1 and NPC2 gene in 34 Niemann–Pick C Italian Patients: identification and structural modeling of novel mutations
Tatiana Fancello, Andrea Dardis, Camillo Rosano, Patrizia Tarugi, Barbara Tappino, Stefania Zampieri, Elisa Pinotti, Fabio Corsolini, Simona Fecarotta, Adele D’Amico, Maja Di Rocco, Graziella Uziel, Sebastiano Calandra, Bruno Bembi, Mirella Filocamo
Novel mutations in the CDKL5 gene, predicted effects and associated phenotypes
S. Russo, M. Marchi, F. Cogliati, M. T. Bonati, M. Pintaudi, E. Veneselli, V. Saletti, M. Balestrini, B. Ben-Zeev, L. Larizza
The spectrum of somatic and germline NF1 mutations in NF1 patients with spinal neurofibromas
Meena Upadhyaya, Gill Spurlock, Lan Kluwe, Nadia Chuzhanova, Emma Bennett, Nick Thomas, Abhijit Guha, Victor Mautner
A new complex homozygous large rearrangement of the PINK1 gene in a Sudanese family with early onset Parkinson’s disease
Cécile Cazeneuve, Channkanira Sân, Salah A. Ibrahim, Maowia M. Mukhtar, Musa M. Kheir, Eric LeGuern, Alexis Brice, Mustafa A. Salih
A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype
C. Pirkevi, S. Lesage, C. Condroyer, H. Tomiyama, N. Hattori, S. Ertan, A. Brice, A. N. Başak