Congenital stationary night blindness: Report of an autosomal recessive family and linkage analysis
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference12 articles.
1. Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness;Bech-Hansen;Nat Genet,2000
2. Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindness;Gal;Nat Genet,1994
3. Congenital stationary night blindness;Haim;Acta Ophthalmol (Copenh),1986
4. Rapid multipoint linkage analysis of recessive traits in nuclear families, including homozygosity mapping;Kruglyak;Am J Hum Genet,1995
5. Homozygosity mapping: A way to map human recessive traits with the DNA of inbred children;Lander;Science,1987
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