Memory disorders (psychiatry)

No evidence of an association between the T16189C mtDNA variant and late onset dementia
A M Gibson, J A Edwardson, D M Turnbull, I G McKeith, C M Morris, P F Chinnery

Journal of Medical Genetics Jan 2004, 41 (1) e7; DOI: 10.1136/jmg.2003.010983
Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (EPM2B) on 6p22
E M Chan, D E Bulman, A D Paterson, J Turnbull, E Andermann, F Andermann, G A Rouleau, A V Delgado-Escueta, S W Scherer, B A Minassian

Journal of Medical Genetics Sep 2003, 40 (9) 671-675; DOI: 10.1136/jmg.40.9.671
Rare polymorphic variants of the AGTR2 gene in boys with non-specific mental retardation
T Bienvenu, K Poirier, H Van Esch, B Hamel, C Moraine, J P Fryns, H H Ropers, C Beldjord, H G Yntema, J Chelly

Journal of Medical Genetics May 2003, 40 (5) 357-359; DOI: 10.1136/jmg.40.5.357
Predictive testing for cognitive functioning in female carriers of the fragile X syndrome using hair root analysis
R Willemsen, A Smits, L-A Severijnen, M Jansen, A Jacobs, E De Bruyn, B Oostra

Journal of Medical Genetics May 2003, 40 (5) 377-379; DOI: 10.1136/jmg.40.5.377
Neuroferritinopathy in a French family with late onset dominant dystonia
P F Chinnery, A R J Curtis, C Fey, A Coulthard, D Crompton, A Curtis, A Lombés, J Burn

Journal of Medical Genetics May 2003, 40 (5) e69; DOI: 10.1136/jmg.40.5.e69
The role of APOE in the phenotypic expression of Leber hereditary optic neuropathy
P Y W Man, C M Morris, M Zeviani, F Carrara, D M Turnbull, P F Chinnery

Journal of Medical Genetics Apr 2003, 40 (4) e41; DOI: 10.1136/jmg.40.4.e41
A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patients
I Longo, S G M Frints, J-P Fryns, I Meloni, C Pescucci, F Ariani, M Borghgraef, M Raynaud, P Marynen, C Schwartz, A Renieri, G Froyen

Journal of Medical Genetics Jan 2003, 40 (1) 11-17; DOI: 10.1136/jmg.40.1.11
Autosomal dominant (AD) pure spastic paraplegia (HSP) linked to locus SPG4 affects almost exclusively males in a large pedigree
A Starling, P Rocco, M R Passos-Bueno, J Hazan, S K Marie, M Zatz

Journal of Medical Genetics Dec 2002, 39 (12) e77; DOI: 10.1136/jmg.39.12.e77
Maternally inherited non-syndromic hearing impairment in a Spanish family with the 7510T>C mutation in the mitochondrial tRNA^Ser(UCN) gene
F J del Castillo, M Villamar, M A Moreno-Pelayo, J J Almela, C Morera, I Adiego, F Moreno, I del Castillo

Journal of Medical Genetics Dec 2002, 39 (12) e82; DOI: 10.1136/jmg.39.12.e82
Identification of novel CLN2 mutations shows Canadian specific NCL2 alleles
W Ju, R Zhong, S Moore, D Moroziewicz, J R Currie, P Parfrey, W T Brown, N Zhong

Journal of Medical Genetics Nov 2002, 39 (11) 822-825; DOI: 10.1136/jmg.39.11.822

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