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author Tuschl, Karin
Clayton, Peter T.
Gospe, Sidney M.
Gulab, Shamshad
Ibrahim, Shahnaz
Singhi, Pratibha
Aulakh, Roosy
Ribeiro, Reinaldo T.
Barsottini, Orlando G.
Zaki, Maha S.
Del Rosario, Maria Luz
Dyack, Sarah
Price, Victoria
Rideout, Andrea
Gordon, Kevin
Wevers, Ron A.
Chong, W.K. ‘‘Kling’’
Mills, Philippa B.
author_facet Tuschl, Karin
Clayton, Peter T.
Gospe, Sidney M.
Gulab, Shamshad
Ibrahim, Shahnaz
Singhi, Pratibha
Aulakh, Roosy
Ribeiro, Reinaldo T.
Barsottini, Orlando G.
Zaki, Maha S.
Del Rosario, Maria Luz
Dyack, Sarah
Price, Victoria
Rideout, Andrea
Gordon, Kevin
Wevers, Ron A.
Chong, W.K. ‘‘Kling’’
Mills, Philippa B.
author_sort Tuschl, Karin
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spelling pubmed-49741052016-08-11 Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man Tuschl, Karin Clayton, Peter T. Gospe, Sidney M. Gulab, Shamshad Ibrahim, Shahnaz Singhi, Pratibha Aulakh, Roosy Ribeiro, Reinaldo T. Barsottini, Orlando G. Zaki, Maha S. Del Rosario, Maria Luz Dyack, Sarah Price, Victoria Rideout, Andrea Gordon, Kevin Wevers, Ron A. Chong, W.K. ‘‘Kling’’ Mills, Philippa B. Am J Hum Genet Correction Elsevier 2016-08-04 2016-08-02 /pmc/articles/PMC4974105/ /pubmed/27486784 http://dx.doi.org/10.1016/j.ajhg.2016.07.015 Text en © 2016 American Society of Human Genetics. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Correction
Tuschl, Karin
Clayton, Peter T.
Gospe, Sidney M.
Gulab, Shamshad
Ibrahim, Shahnaz
Singhi, Pratibha
Aulakh, Roosy
Ribeiro, Reinaldo T.
Barsottini, Orlando G.
Zaki, Maha S.
Del Rosario, Maria Luz
Dyack, Sarah
Price, Victoria
Rideout, Andrea
Gordon, Kevin
Wevers, Ron A.
Chong, W.K. ‘‘Kling’’
Mills, Philippa B.
Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man
title Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man
title_full Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man
title_fullStr Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man
title_full_unstemmed Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man
title_short Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man
title_sort syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused by mutations in slc30a10, a manganese transporter in man
topic Correction
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974105/
https://www.ncbi.nlm.nih.gov/pubmed/27486784
http://dx.doi.org/10.1016/j.ajhg.2016.07.015
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