Genetics of the neuronal ceroid lipofuscinoses (Batten disease)-Reference-Cited by-同舟云学术

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Genetics of the neuronal ceroid lipofuscinoses (Batten disease)

Published:2015-10 Issue:10 Volume:1852 Page:2237-2241
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Mole Sara E.,Cotman Susan L.

Funder

UK Batten Disease Family Association

USA Batten Disease Support and Research Association

National Institutes of Health: National Institute of Neurological Disorders & Stroke

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference39 articles.

1. Mutations in DNAJC5, encoding cysteine-string protein alpha, cause autosomal-dominant adult-onset neuronal ceroid lipofuscinosis;Noskova;Am. J. Hum. Genet.,2011

2. A novel CLN8 mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological function;Vantaggiato;Hum. Mutat.,2009

3. Progranulin is expressed within motor neurons and promotes neuronal cell survival;Ryan;BMC Neurosci.,2009

4. Experimental Therapies in the Neuronal Ceroid Lipofuscinoses;Neverman;Biochim. Biophys. Acta,2015

5. Cell biology of the NCL proteins: what they do and don't do;Cárcel-Trullols;Biochim. Biophys. Acta,2015

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