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The first inborn error of manganese metabolism caused by mutations in SLC30A10, a newly identified manganese transporter

✍ Scribed by Tuschl, K; Clayton, PT; Gospe, SM; Shamshad, G; Ibrahim, S; Singhi, P; Ribeiro, RT; Zaki, MS; del Rosario, M Luz; Dyack, S; Price, V; Wevers, RA; Mills, PB


Book ID
123555059
Publisher
The Lancet
Year
2013
Tongue
English
Weight
53 KB
Volume
381
Category
Article
ISSN
0140-6736

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