Lisbet K. Lind

Myopathy with lactic acidosis is linked to chromosome 12q23.3-24.11 and caused by an intron mutation in the ISCU gene resulting in a splicing defect

Anna Olsson, Lisbet K. Lind, Lars‐Eric Thornell et al. · Human Molecular Genetics · 2008 · 114 citations

Molecular cloning and characterization of the ctpA gene encoding a carboxyl-terminal processing protease. Analysis of a spontaneous photosystem II-deficient mutant strain of the cyanobacterium Synechocystis sp. PCC 6803.

P. R. Anbudurai, Gulshan Stanbekova, Lisbet K. Lind et al. · Journal of Biological Chemistry · 1994 · 103 citations · Full text

Sk18 Mutant Strain, Photobiology, Molecular Biology +18

Mutations in AQP5, Encoding a Water-Channel Protein, Cause Autosomal-Dominant Diffuse Nonepidermolytic Palmoplantar Keratoderma

Diana C. Blaydon, Lisbet K. Lind, Vincent Plagnol et al. · The American Journal of Human Genetics · 2013 · 94 citations · Full text

Genetic Disorder, Genetics, Water-channel Protein +4

Acclimation Processes in the Light-Harvesting System of the Cyanobacterium <i>Anacystis nidulans</i> following a Light Shift from White to Red Light

Anders Lönneborg, Lisbet K. Lind, Shubhangi Kalla et al. · PLANT PHYSIOLOGY · 1985 · 88 citations · Full text

The CTLA4 region as a general autoimmunity factor: An extended pedigree provides evidence for synergy with the HLA locus in the etiology of type 1 diabetes mellitus, Hashimoto's thyroiditis and Graves' disease

Elísabet Einarsdóttir, Ingegerd Söderström, Anna Löfgren‐Burström et al. · European Journal of Human Genetics · 2003 · 63 citations · Full text

Histocompatibility, Type 1, Immunogenetics +12