Literature DB >> 2280973

Localization of the X-linked ocular albinism gene (OA1) between DXS278/DXS237 and DXS143/DXS16 by linkage analysis.

A A Bergen1, C Samanns, D B Van Dorp, M A Ferguson-Smith, A Gal, E M Bleeker-Wagemakers.   

Abstract

Linkage analysis was performed in six families segregating for X-linked ocular albinism of the Nettleship-Falls type using four polymorphic DNA markers from the distal Xp. Linkage was found between the disease locus (OA1) and the loci DXS237 (theta max = 0.06, Zmax = 2.82), DXS278 (theta max = 0.03, Zmax = 5.27) and DXS16 (theta max = 0.10, Zmax = 2.33). The analysis of multiple informative meioses suggests that OA1 maps between DXS278/DXS237 and DXS143/DXS16. Multipoint linkage analysis slightly favours the order DXS278/DXS237-OA1-DXS16. These data refine the genetic localization of OA1 and may be useful for carrier detection in X-linked ocular albinism by DNA analysis.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2280973     DOI: 10.3109/13816819009020975

Source DB:  PubMed          Journal:  Ophthalmic Paediatr Genet        ISSN: 0167-6784


  5 in total

1.  Genetic mapping of X linked ocular albinism: linkage analysis in British families.

Authors:  S J Charles; A T Moore; J R Yates
Journal:  J Med Genet       Date:  1992-08       Impact factor: 6.318

2.  Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type.

Authors:  A A Bergen; C Samanns; E J Schuurman; L van Osch; D B van Dorp; A J Pinckers; E Bakker; A Gal; G J van Ommen; E M Bleeker-Wagemakers
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

Review 3.  Albinism: modern molecular diagnosis.

Authors:  S M Carden; R E Boissy; P J Schoettker; W V Good
Journal:  Br J Ophthalmol       Date:  1998-02       Impact factor: 4.638

4.  Phenotypic variability in X-linked ocular albinism: relationship to linkage genotypes.

Authors:  R E Schnur; P A Wick; C Bailey; T Rebbeck; R G Weleber; J Wagstaff; A W Grix; R A Pagon; A Hockey; M J Edwards
Journal:  Am J Hum Genet       Date:  1994-09       Impact factor: 11.025

5.  Deep intronic GPR143 mutation in a Japanese family with ocular albinism.

Authors:  Takuya Naruto; Nobuhiko Okamoto; Kiyoshi Masuda; Takao Endo; Yoshikazu Hatsukawa; Tomohiro Kohmoto; Issei Imoto
Journal:  Sci Rep       Date:  2015-06-10       Impact factor: 4.379

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.