Literature DB >> 9529339

Evidence for genetic heterogeneity in X-linked congenital stationary night blindness.

K M Boycott1, W G Pearce, M A Musarella, R G Weleber, T A Maybaum, D G Birch, Y Miyake, R S Young, N T Bech-Hansen.   

Abstract

X-linked congenital stationary night blindness (CSNB) is a nonprogressive retinal disorder characterized by disturbed or absent night vision; its clinical features may also include myopia, nystagmus, and impaired visual acuity. X-linked CSNB is clinically heterogeneous, and it may also be genetically heterogeneous. We have studied 32 families with X-linked CSNB, including 11 families with the complete form of CSNB and 21 families with the incomplete form of CSNB, to identify genetic-recombination events that would refine the location of the disease genes. Critical recombination events in the set of families with complete CSNB have localized a disease gene to the region between DXS556 and DXS8083, in Xp11.4-p11.3. Critical recombination events in the set of families with incomplete CSNB have localized a disease gene to the region between DXS722 and DXS8023, in Xp11.23. Further analysis of the incomplete-CSNB families, by means of disease-associated-haplotype construction, identified 17 families, of apparent Mennonite ancestry, that share portions of an ancestral chromosome. Results of this analysis refined the location of the gene for incomplete CSNB to the region between DXS722 and DXS255, a distance of 1.2 Mb. Genetic and clinical analyses of this set of 32 families with X-linked CSNB, together with the family studies reported in the literature, strongly suggest that two loci, one for complete (CSNB1) and one for incomplete (CSNB2) X-linked CSNB, can account for all reported mapping information.

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Year:  1998        PMID: 9529339      PMCID: PMC1377021          DOI: 10.1086/301781

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  40 in total

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Review 3.  Disease gene mapping in isolated human populations: the example of Finland.

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Authors:  A Gal; U Orth; W Baehr; E Schwinger; T Rosenberg
Journal:  Nat Genet       Date:  1994-05       Impact factor: 38.330

6.  Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map.

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7.  Integrated human genome-wide maps constructed using the CEPH reference panel.

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8.  Identification of a key recombinant which assigns the incomplete congenital stationary night blindness gene proximal to MAOB.

Authors:  A A Bergen; P Kestelyn; M Leys; F Meire
Journal:  J Med Genet       Date:  1994-07       Impact factor: 6.318

9.  Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness.

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Journal:  Nature       Date:  1994-02-17       Impact factor: 49.962

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7.  Spectrum of Cav1.4 dysfunction in congenital stationary night blindness type 2.

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8.  Gain-of-function nature of Cav1.4 L-type calcium channels alters firing properties of mouse retinal ganglion cells.

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10.  A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation.

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