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Putative association of a mutant ROM1 allele with retinitis pigmentosa

✍ Scribed by Amalia Martínez-Mir; Concha Vilela; Mònica Bayés; Diana Valverde; L. Dain; Magdalena Beneyto; Marina Marco; Montserrat Baiget; Daniel Grinberg; Susana Balcells; Roser Gonzàlez-Duarte; Lluïsa Vilageliu

Book ID
106136671
Publisher
Springer
Year
1997
Tongue
English
Weight
34 KB
Volume
99
Category
Article
ISSN
0340-6717

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✍ Dieuwke B. Dorp; Alan F. Wright; Andrew D. Carothers; Elizabeth M. Bleeker-Wagem 📂 Article 📅 1992 🏛 Springer 🌐 English ⚖ 446 KB

The results of linkage analysis in a family with X-linked retinitis pigmentosa (XLRP) are presented. Probe M27B (DXS255), localised to Xpll.22, was only loosely linked to XLRP, whereas pHOC3 (OTC), in the more distal Xp21.1 region, was tightly linked. In this family, the conditional probability of a