| Literature DB >> 10953198 |
V Holmberg1, L Lauronen, T Autti, P Santavuori, M Savukoski, P Uvebrant, I Hofman, L Peltonen, I Järvelä.
Abstract
The authors analyzed the clinical phenotype, including MRI, of eight patients with Finnish variant late infantile neuronal ceroid lipofuscinosis (vLINCLFin; CLN5; MIM256731). Although the four known mutations, including one novel mutation identified in this study, have very different consequences for the predicted polypeptide, none of them results in an atypical phenotype, as has been reported in other forms of NCL. Thus, it seems likely that each mutation severely disturbs the normal function of the CLN5 protein.Entities:
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Year: 2000 PMID: 10953198 DOI: 10.1212/wnl.55.4.579
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910