Pages that link to "Q24679383"

The following pages link to Tay-Sachs disease in Moroccan Jews: deletion of a phenylalanine in the alpha-subunit of beta-hexosaminidase (Q24679383):

Displaying 7 items.

• A mutation in a mild form of galactosialidosis impairs dimerization of the protective protein and renders it unstable (Q24564644) (← links)
• The molecular basis of HEXA mRNA deficiency caused by the most common Tay-Sachs disease mutation (Q24673000) (← links)
• Cloning and sequence analysis of a cDNA encoding the alpha-subunit of mouse beta-N-acetylhexosaminidase and comparison with the human enzyme (Q31170911) (← links)
• Alternative splicing of RNA triplets is often regulated and accelerates proteome evolution (Q34123419) (← links)
• Familial Mediterranean fever (FMF) in Moroccan Jews: demonstration of a founder effect by extended haplotype analysis (Q35195069) (← links)
• Linkage disequilibrium mapping places the gene causing familial Mediterranean fever close to D16S246. (Q35881476) (← links)
• Beta-hexosaminidase splice site mutation has a high frequency among non-Jewish Tay-Sachs disease carriers from the British Isles (Q41642105) (← links)