Hereditary spastic paraplegia: mitochondrial metalloproteases of yeast D. A. Pearce Review article Pages: 443 - 448
Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies R. AllikmetsJohanna M. SeddonKonstantin Petrukhin Rapid communication Pages: 449 - 453
NME6: a new member of the nm23/nucleoside diphosphate kinase gene family located on human chromosome 3p21.3 James G. MehusPanagiotis DeloukasD. O. Lambeth Rapid communication Pages: 454 - 459
A mitochondrial cytochrome b mutation but no mutations of nuclearly encoded subunits in ubiquinol cytochrome c reductase (complex III) deficiency Isabelle ValnotJohanna KassisAgnès Rötig Original investigation Pages: 460 - 466
Gene expression patterns in cell lines from patients with 18q– syndrome Zhiqiang WangJannine D. CodyP. O’Connell Original investigation Pages: 467 - 475
Hyperinsulinism-hyperammonemia syndrome caused by mutant glutamate dehydrogenase accompanied by novel enzyme kinetics T. YorifujiJunko MuroiToru Momoi Original investigation Pages: 476 - 479
Genetic anticipation in Portuguese kindreds with familial amyloidotic polyneuropathy is unlikely to be caused by triplet repeat expansions Miguel SoaresJoel BuxbaumMaria João Saraiva Original investigation Pages: 480 - 485
Ancestral origin of variation in the triosephosphate isomerase gene promoter A. HumphriesA. AtionuD. M. Layton Original investigation Pages: 486 - 491
Association of the human NPPS gene with ossification of the posterior longitudinal ligament of the spine (OPLL) Isao NakamuraShiro IkegawaY. Nakamura Original investigation Pages: 492 - 497
Molecular cloning and characterization of the human NUDC gene Naomichi MatsumotoD. H. Ledbetter Original investigation Pages: 498 - 504
Comparison of complementary and genomic DNA sequencing for the detection of mutations in the HMBS gene in British patients with acute intermittent porphyria: identification of 25 novel mutations Sharon D. WhatleyJackie R. WoolfG. H. Elder Original investigation Pages: 505 - 510
Two novel mutations in a cystic fibrosis patient of Chinese origin John A. WagnerAthina VassilakisJ. J. Wine Original investigation Pages: 511 - 515
Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases Miguel Angel PujanaJordi CorralThe Ataxia Study Group Original investigation Pages: 516 - 522
Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine : glyoxylate aminotransferase gene Doroti PirulliDaniela PuzzerFiorella Florian Short report Pages: 523 - 525
Intragenic polymorphic missense mutations in the XLRS1 gene in families with juvenile X-linked retinoschisis Miki HiraokaMichael T. TreseB. S. Shastry Letter to the editor Pages: 526 - 527
