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Beta-hexosaminidase splice site mutation has a high frequency among non-Jewish Tay-Sachs disease carriers from the British Isles.

In the course of defining mutations causing Tay-Sachs disease (TSD) in non-Jewish patients and carriers from the British Isles, we identified a guanine to adenine change (also previously described) in the obligatory GT sequence of the donor splice site at the 5' end of intron 9 of the hexosamin...

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Библиографические подробности
Главные авторы: Landels, E C, Green, P M, Ellis, I H, Fensom, A H, Bobrow, M
Формат: Artigo
Язык:Inglês
Опубликовано: 1992
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Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC1016063/
https://ncbi.nlm.nih.gov/pubmed/1387685
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