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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| Autori principali: | , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BMC
2007-06-01
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| Serie: | BMC Cell Biology |
| Accesso online: | http://www.biomedcentral.com/1471-2121/8/22 |
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