Hakuluettelo:
Käännös:
Wolman disease (suomeksi)
- Määritelmät:
- A rare genetic disorder caused by deficiency of an enzyme known as lysosomal acid lipase (LAL or LIPA), necessary to break down certain lipids.
Viimeisimmät haut: Wolman disease, nonpermeabilizing, replottings, orders of council, banjars, judgecraft