Glycosylation, transport, and complex formation of palmitoyl protein thioesterase 1 (PPT1) – distinct characteristics in neurons

<p>Abstract</p> <p>Background</p> <p>Neuronal ceroid lipofuscinoses (NCLs) are collectively the most common type of recessively inherited childhood encephalopathies. The most severe form of NCL, infantile neuronal ceroid lipofuscinosis (INCL), is caused by mutations in the <it>CLN1 </it>gene, result...

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Hauptverfasser:	Jauhiainen Matti, Saarela Jani, Kopra Outi, Salonen Tarja, von Schantz Carina, Lyly Annina, Kyttälä Aija, Jalanko Anu
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	BMC 2007-06-01
Schriftenreihe:	BMC Cell Biology
Online-Zugang:	http://www.biomedcentral.com/1471-2121/8/22
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