Development of a 1.4-Mb BAC/PAC Contig and Physical Map within the Critical Region for Complete X-Linked Congenital Stationary Night Blindness in Xp11.4
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference11 articles.
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2. Integration of 101 DNA markers across human Xp11 using a panel of somatic cell hybrids;Boycott;Cytogenet. Cell Genet.,1997
3. Evidence for genetic heterogeneity in X-linked congenital stationary night blindness;Boycott;Am. J. Hum. Genet.,1998
4. Construction of a 1.5-Mb bacterial artificial chromosome contig in Xp11.23, a region of high gene content;Boycott;Genomics,1998
5. The location of human CASK at Xp11.4 identifies this gene as a candidate for X-linked optic atrophy;Dimitratos;Genomics,1998
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1. Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness;Nature Genetics;2000-11
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