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- j.ajhg.2011.11.030 doi "10.1016/j.ajhg.2011.11.030".
- j.ajhg.2011.11.030 first1 "P.".
- j.ajhg.2011.11.030 first10 "C.".
- j.ajhg.2011.11.030 first11 "U.".
- j.ajhg.2011.11.030 first12 "R.".
- j.ajhg.2011.11.030 first13 "S.".
- j.ajhg.2011.11.030 first14 "O.".
- j.ajhg.2011.11.030 first15 "G.".
- j.ajhg.2011.11.030 first16 "P.".
- j.ajhg.2011.11.030 first17 "S.".
- j.ajhg.2011.11.030 first18 "L. B.".
- j.ajhg.2011.11.030 first19 "S. G.".
- j.ajhg.2011.11.030 first2 "C.".
- j.ajhg.2011.11.030 first20 "J.".
- j.ajhg.2011.11.030 first3 "V.".
- j.ajhg.2011.11.030 first4 "G. C.".
- j.ajhg.2011.11.030 first5 "I.".
- j.ajhg.2011.11.030 first6 "P.".
- j.ajhg.2011.11.030 first7 "J.".
- j.ajhg.2011.11.030 first8 "M.".
- j.ajhg.2011.11.030 first9 "G.".
- j.ajhg.2011.11.030 isCitedBy SLC33A1.
- j.ajhg.2011.11.030 issue "1".
- j.ajhg.2011.11.030 journal "The American Journal of Human Genetics".
- j.ajhg.2011.11.030 last1 "Huppke".
- j.ajhg.2011.11.030 last10 "Wilson".
- j.ajhg.2011.11.030 last11 "Gruber-Sedlmayr".
- j.ajhg.2011.11.030 last12 "Ullmann".
- j.ajhg.2011.11.030 last13 "Haas".
- j.ajhg.2011.11.030 last14 "Elpeleg".
- j.ajhg.2011.11.030 last15 "Nürnberg".
- j.ajhg.2011.11.030 last16 "Nürnberg".
- j.ajhg.2011.11.030 last17 "Dad".
- j.ajhg.2011.11.030 last18 "Møller".
- j.ajhg.2011.11.030 last19 "Kaler".
- j.ajhg.2011.11.030 last2 "Brendel".
- j.ajhg.2011.11.030 last20 "Gärtner".
- j.ajhg.2011.11.030 last3 "Kalscheuer".
- j.ajhg.2011.11.030 last4 "Korenke".
- j.ajhg.2011.11.030 last5 "Marquardt".
- j.ajhg.2011.11.030 last6 "Freisinger".
- j.ajhg.2011.11.030 last7 "Christodoulou".
- j.ajhg.2011.11.030 last8 "Hillebrand".
- j.ajhg.2011.11.030 last9 "Pitelet".
- j.ajhg.2011.11.030 pages "61–68".
- j.ajhg.2011.11.030 pmc "3257879".
- j.ajhg.2011.11.030 pmid "22243965".
- j.ajhg.2011.11.030 title "Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin".
- j.ajhg.2011.11.030 volume "90".
- j.ajhg.2011.11.030 year "2012".