Deregulation of subcellular biometal homeostasis through loss of the metal transporter, Zip7, in a childhood neurodegenerative disorder-Reference-Cited by-同舟云学术

Deregulation of subcellular biometal homeostasis through loss of the metal transporter, Zip7, in a childhood neurodegenerative disorder

Published:2014-02-28 Issue:1 Volume:2 Page:
ISSN:2051-5960
Container-title:Acta Neuropathologica Communications
language:en
Short-container-title:acta neuropathol commun

Author:

Grubman Alexandra,Lidgerwood Grace E,Duncan Clare,Bica Laura,Tan Jiang-Li,Parker Sarah J,Caragounis Aphrodite,Meyerowitz Jodi,Volitakis Irene,Moujalled Diane,Liddell Jeffrey R,Hickey James L,Horne Malcolm,Longmuir Shoshanah,Koistinaho Jari,Donnelly Paul S,Crouch Peter J,Tammen Imke,White Anthony R,Kanninen Katja M

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Clinical Neurology,Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1186/2051-5960-2-25.pdf

Reference68 articles.

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3. Kousi M, Lehesjoki AE, Mole SE: Update of the mutation spectrum and clinical correlations of over 360 mutations in eight genes that underlie the neuronal ceroid lipofuscinoses. Hum Mutat 2012, 33: 42–63. 10.1002/humu.21624

4. Chen R, Fearnley IM, Palmer DN, Walker JE: Lysine 43 is trimethylated in subunit C from bovine mitochondrial ATP synthase and in storage bodies associated with batten disease. J Biol Chem 2004, 279: 21883–21887. 10.1074/jbc.M402074200

5. Haltia M: The neuronal ceroid-lipofuscinoses: from past to present. Biochimica Et Biophysica Acta 2006, 1762: 850–856. 10.1016/j.bbadis.2006.06.010

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