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Autor:
Litsa Karageorgos, Leanne Hein, Tina Rozaklis, Melissa Adams, Stephen Duplock, Marten Snel, Kim Hemsley, Tim Kuchel, Nicholas Smith, John J. Hopwood
Publikováno v:
Neurobiology of Disease, Vol 91, Iss , Pp 143-154 (2016)
Gaucher disease arises from mutations in the β-glucocerebrosidase gene which encodes an enzyme required for the lysosomal catabolism of glucosylceramide. We have identified a naturally occurring mutation in the β-glucocerebrosidase gene in sheep th
Externí odkaz:
https://doaj.org/article/dbd473fdfc5f44738c17397641270c4e