Associated Papers
A Neurodegenerative Phenotype Associated With Sjögren-Larsson Syndrome.
Warrack S et al.
Journal of Child Neurology, 2021
Novel mutations and a severe neurological phenotype in Sjögren-Larsson syndrome patients from Iran.
Kariminejad A et al.
European Journal of Medical Genetics, 2018
Sjögren-Larsson syndrome: diversity of mutations and polymorphisms in the fatty aldehyde dehydrogenase gene (ALDH3A2).
Rizzo WB et al.
Human Mutation, 2005
The molecular basis of Sjögren-Larsson syndrome: mutation analysis of the fatty aldehyde dehydrogenase gene.
Rizzo WB et al.
American Journal of Human Genetics, 1999
Spectrum of mutations and sequence variants in the FALDH gene in patients with Sjögren-Larsson syndrome.
Sillén A et al.
Human Mutation, 1998
Select a paper to view details