Erratum: Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man (American Journal of Human Genetics (2012) 90 (457–466) (S0002929712000523) (10.1016/j.ajhg.2012.01.018));Syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused by mutations in SLC30A10, a manganese transporter in man

American Journal of Human Genetics

Volumn 90, Issue 3, 2012, Pages 457-466

  Tuschl, Karin ^a   Clayton, Peter T ^a   Gospe Jr , Sidney M ^b   Gulab, Shamshad ^c   Ibrahim, Shahnaz ^c   Singhi, Pratibha ^d   Aulakh, Roosy ^e   Ribeiro, Reinaldo T ^f   Barsottini, Orlando G ^f   Zaki, Maha S ^g   Del Rosario, Maria Luz ^h   Dyack, Sarah ⁱ   Price, Victoria ⁱ   Rideout, Andrea ⁱ   Gordon, Kevin ⁱ   Wevers, Ron A ^j   Kling Chong, W K ^k   Mills, Philippa B ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b UNIVERSITY OF WASHINGTON   (United States)

^c AGA KHAN UNIVERSITY HOSPITAL   (Pakistan)

^d POSTGRADUATE INSTITUTE OF MEDICAL EDUCATION AND RESEARCH   (India)

^e GOVERNMENT MEDICAL COLLEGE AND HOSPITAL   (India)

^f FEDERAL UNIVERSITY OF SÃO PAULO   (Brazil)

^g NATIONAL RESEARCH CENTRE   (Egypt)

^h Institute of Urology   (Philippines)

ⁱ IWK HEALTH CENTRE   (Canada)

^j RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^k Hospital for Children NHS Trust   (United Kingdom)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ABNORMALLY HIGH SUBSTRATE CONCENTRATION IN BLOOD; ADOLESCENT; ADULT; ARTICLE; CHILD; DYSTONIA; FEMALE; FUNGAL STRAIN; GENE; GENE MAPPING; GENE MUTATION; GENE SEQUENCE; HOMOZYGOSITY; HUMAN; HYPERMANGANESEMIA; LIVER CIRRHOSIS; MALE; NONHUMAN; POLYCYTHEMIA; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SLC30A10 GENE; YEAST;

PARKINSONIA;

EID: 84858078704     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2016.07.015     Document Type: Erratum

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