Publisher Correction: Spermine synthase deficiency causes lysosomal dysfunction and oxidative stress in models of Snyder-Robinson syndrome.

Li, Chong; Brazill, Jennifer M; Liu, Sha; Bello, Christofer; Zhu, Yi; Morimoto, Marie; Cascio, Lauren; Pauly, Rini; Diaz-Perez, Zoraida; Malicdan, May Christine V; Wang, Hongbo; Boccuto, Luigi; Schwartz, Charles E; Gahl, William A; Boerkoel, Cornelius F; Zhai, R Grace

Li, Chong; Brazill, Jennifer M; Liu, Sha; Bello, Christofer; Zhu, Yi; Morimoto, Marie; Cascio, Lauren; Pauly, Rini; Diaz-Perez, Zoraida; Malicdan, May Christine V; Wang, Hongbo; Boccuto, Luigi; Schwartz, Charles E; Gahl, William A; Boerkoel, Cornelius F; Zhai, R Grace.

Afiliação

Li C; Department of Molecular and Cellular Pharmacology, University of Miami Miller School of Medicine, 33136, Miami, FL, USA.
Brazill JM; Department of Molecular and Cellular Pharmacology, University of Miami Miller School of Medicine, 33136, Miami, FL, USA.
Liu S; School of Pharmacy, Key Laboratory of Molecular Pharmacology and Drug Evaluation (Yantai University), Ministry of Education, Collaborative Innovation Center of Advanced Drug Delivery System and Biotech Drugs in Universities of Shandong, Yantai University, 264005, Yantai, Shandong, China.
Bello C; Department of Molecular and Cellular Pharmacology, University of Miami Miller School of Medicine, 33136, Miami, FL, USA.
Zhu Y; Department of Molecular and Cellular Pharmacology, University of Miami Miller School of Medicine, 33136, Miami, FL, USA.
Morimoto M; NIH Undiagnosed Diseases Program, National Human Genome Research Institute, NIH, 20892, Bethesda, MD, USA.
Cascio L; Section of Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, NIH, 20892, Bethesda, MD, USA.
Pauly R; JC Self Research Institute, Greenwood Genetic Center, 29646, Greenwood, SC, USA.
Diaz-Perez Z; JC Self Research Institute, Greenwood Genetic Center, 29646, Greenwood, SC, USA.
Malicdan MCV; Department of Molecular and Cellular Pharmacology, University of Miami Miller School of Medicine, 33136, Miami, FL, USA.
Wang H; NIH Undiagnosed Diseases Program, National Human Genome Research Institute, NIH, 20892, Bethesda, MD, USA.
Boccuto L; Section of Human Biochemical Genetics, Medical Genetics Branch, National Human Genome Research Institute, NIH, 20892, Bethesda, MD, USA.
Schwartz CE; Office of the Clinical Director, National Human Genome Research Institute, NIH, 20892, Bethesda, MD, USA.
Gahl WA; School of Pharmacy, Key Laboratory of Molecular Pharmacology and Drug Evaluation (Yantai University), Ministry of Education, Collaborative Innovation Center of Advanced Drug Delivery System and Biotech Drugs in Universities of Shandong, Yantai University, 264005, Yantai, Shandong, China.
Boerkoel CF; JC Self Research Institute, Greenwood Genetic Center, 29646, Greenwood, SC, USA.
Zhai RG; JC Self Research Institute, Greenwood Genetic Center, 29646, Greenwood, SC, USA.

Nat Commun ; 9(1): 337, 2018 01 18.

Article em En | MEDLINE | ID: mdl-29348635

ABSTRACT

ABSTRACT

The originally published version of this Article contained errors in Figure 1. In panel c, the grey shading denoting evolutionary conservation and the arrowheads indicating amino acids affected in Snyder-Robinson syndrome were displaced relative to the sequence. These errors have now been corrected in both the PDF and HTML versions of the manuscript.

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Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Etiology_studies Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos

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