| Literature DB >> 11493318 |
K Becker1, M Csikós, A Horváth, S Kárpáti.
Abstract
The X-linked dominant Conradi-Hünermann-Happle (CDPX2, MIM 302960) syndrome belongs to the rare, heterogeneous group of diseases called chondrodysplasia punctata. The disease has been connected recently with deficiency of 3beta-hydroxysteroid-Delta8-Delta7-isomerase (also called emopamil-binding protein, EBP), catalysing an intermediate step in the conversion of lanosterol to cholesterol (1, 2). We report a case of CDPX2 with a new missense mutation (C-->G 439) in exon 4, leading to a R147G aminoacid substitution in the EBP.Entities:
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Year: 2001 PMID: 11493318 DOI: 10.1034/j.1600-0625.2001.100409.x
Source DB: PubMed Journal: Exp Dermatol ISSN: 0906-6705 Impact factor: 3.960