bibliographic entry 6395178 [be/6395178]
https://w3id.org/oc/corpus/be/6395178

is a
content
  • Tuschl, K, Clayton, P.T, Gospe, S.M, Jr, Gulab, S, Ibrahim, S, Singhi, P, Aulakh, R, Ribeiro, R.T, Barsottini, O.G, Zaki, M.S. Syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused by mutations in SLC30A10, a manganese transporter in man, Am. J. Hum. Genet, 2012, 90, 457, 466, DOI: 10.1016/j.ajhg.2012.01.018, PMID: 22341972
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