Further investigation of the HEXA gene intron 9 donor splice site mutation frequently found in non-Jewish Tay-Sachs disease patients from the British Isles.

Ítems similars

• Beta-hexosaminidase splice site mutation has a high frequency among non-Jewish Tay-Sachs disease carriers from the British Isles.
  per: Landels, E C, et al.
  Publicat: (1992)
• Frequency of the Tay-Sachs disease splice and insertion mutations in the UK Ashkenazi Jewish population.
  per: Landels, E C, et al.
  Publicat: (1991)
• Tay-Sachs disease heterozygote detection: use of a centrifugal analyser for automation of hexosaminidase assays with two different artificial substrates.
  per: Landels, E C, et al.
  Publicat: (1991)
• Tay-Sachs disease: high gene frequency in a non-Jewish population.
  per: Kelly, T E, et al.
  Publicat: (1975)
• Novel mutations and DNA-based screening in non-Jewish carriers of Tay-Sachs disease.
  per: Akerman, B R, et al.
  Publicat: (1997)