| Literature DB >> 10444339 |
J Thoene1, R Lemons, Y Anikster, J Mullet, K Paelicke, C Lucero, W Gahl, J Schneider, S G Shu, H T Campbell.
Abstract
Six patients with the intermediate form of cystinosis are described. Two have new mutations not previously described. The disease occurs due either to the combination of one mild mutation and one which is known to cause nephropathic cystinosis or to homozygosity for a predicted mild mutation. Partial phenotypic correction of cystinotic fibroblasts by transfection with normal cDNA or a cDNA derived from a mutation causing intermediate cystinosis is demonstrated. Copyright 1999 Academic Press.Entities:
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Year: 1999 PMID: 10444339 DOI: 10.1006/mgme.1999.2876
Source DB: PubMed Journal: Mol Genet Metab ISSN: 1096-7192 Impact factor: 4.797