Accumulation of glial fibrillary acidic protein and histone H4 in brain storage bodies of Tibetan terriers with hereditary neuronal ceroid lipofuscinosis-Reference-Cited by-同舟云学术

Accumulation of glial fibrillary acidic protein and histone H4 in brain storage bodies of Tibetan terriers with hereditary neuronal ceroid lipofuscinosis

Published:2007-11 Issue:6 Volume:30 Page:952-963
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Katz M. L.,Sanders D. N.,Mooney B. P.,Johnson Gary S.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://www.springerlink.com/index/pdf/10.1007/s10545-007-0683-y

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3. Awano T, Katz ML, Sohar I, et al (2006b) A frame shift mutation in the canine ortholog of human CLN2 in a juvenile dachshund with neuronal ceroid lipofuscinosis. Mol Genet Metab 89: 254-60.

4. Buzy A, Ryan EM, Jennings KR, Palmer DN, Griffiths DE (1996) Use of electrospray ionization mass spectrometry to study binding of F0 inhibitors to ceroid lipofuscinosis protein, a model system for subunit c of mitochondrial ATP synthase. Rapid Commun Mass Spectrom 10: 790-96.

5. Condorelli DF, Nicoletti VG, Barresi V, et al (1999) Structural features of the rat GFAP gene and identification of a novel alternative transcript. J Neurosci Res 56: 219-28.

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