Skip to Main Content

Paper Details

Structural basis for the dominant or recessive character of GLIALCAM mutations found in leukodystrophies.
Hum Mol Genet
10
2020
GLIALCAM, GLIALCAM genes, GLIALCAM mutations, GlialCAM, GlialCAM molecules, Ig, Ig domain, MLC, MLC1, MLC2A, MLC2B, Megalencephalic leukoencephalopathy with subcortical cysts, anti-GlialCAM, astrocyte junctions, astrocyte-, cysteine, immunoglobulin, leukodystrophies, leukodystrophy, neighbouring cells, patients, white matter edema
Author NameAffiliation
Juan Fern??ndez-Recio
Juan Fern??ndez-RecioInstitut de Biologia Molecular de Barcelona
Juan Fern??ndez-RecioInstituto de Ciencias de la Vid y del Vino (ICVV), CSIC- Universidad de La Rioja- Gobierno de la Rioja
Juan Fern??ndez-Recio
Juan Fern??ndez-RecioInstitut de Biologia Molecular de Barcelona
Juan Fern??ndez-RecioInstituto de Ciencias de la Vid y del Vino (ICVV), CSIC- Universidad de La Rioja- Gobierno de la Rioja
  • 1 - 6

Datasets

Release 1.2