| Literature DB >> 9598732 |
M E Porteous1, L Strain, L J Logie, R M Herd, E C Benton.
Abstract
Keratosis follicularis spinulosa decalvans (KFSD) is a rare, X linked disorder with skin and eye involvement (MIM 308800). We have studied a large British family with KFSD using polymorphic markers from Xp21-p23 and obtained a lod score of 2.056 at theta=0 with markers proximal and distal to the KFSD candidate region Xp22.13-p22.2 identified by Oosterwijk et al. Our data confirm the linkage to Xp22.13-p22.2 observed in the previously reported Dutch family, but fail to narrow the candidate interval for the KFSD locus.Entities:
Mesh:
Year: 1998 PMID: 9598732 PMCID: PMC1051286 DOI: 10.1136/jmg.35.4.336
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318