X-Linked Cone-Rod Dystrophy (Locus COD1): Identification of Mutations in RPGR Exon ORF15-Reference-Cited by-同舟云学术

X-Linked Cone-Rod Dystrophy (Locus COD1): Identification of Mutations in RPGR Exon ORF15

Published:2002-04 Issue:4 Volume:70 Page:1049-1053
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Demirci F. Yesim K.,Rigatti Brian W.,Wen Gaiping,Radak Amy L.,Mah Tammy S.,Baic Corrine L.,Traboulsi Elias I.,Alitalo Tiina,Ramser Juliane,Gorin Michael B.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference25 articles.

1. Cone dystrophy (X-linked) (COD1) maps between DXS7 (L1.28) and DXS206 (Xj1.1) and is linked to DXS84 (754);Bartley;Cytogenet Cell Genet,1989

2. DNA carrier detection in X-linked progressive cone dystrophy;Bergen;Clin Genet,1994

3. Additional evidence for a gene locus for progressive cone dystrophy with late rod involvement in Xp21.1-p11.3;Bergen;Genomics,1993

4. Localization of a novel X-linked progressive cone dystrophy gene to Xq27: evidence for genetic heterogeneity;Bergen;Am J Hum Genet,1997

5. X-linked retinitis pigmentosa;Bird;Br J Ophthalmol,1975

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