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Autor:
Alexander T. Young, Kien N. Ly, Callum Wilson, Klaus Lehnert, Russell G. Snell, Suzanne J. Reid, Jessie C. Jacobsen
Publikováno v:
Disease Models & Mechanisms, Vol 11, Iss 11 (2018)
Brain dopamine-serotonin vesicular transport disease is a rare disease caused by autosomal recessive mutations in the SLC18A2 gene, which encodes the VMAT2 protein. VMAT2 is a membrane protein responsible for vesicular transport of monoamines, and it
Externí odkaz:
https://doaj.org/article/fae458ff799740f39e42bfda3ada7ec0