Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1).
about
X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F geneEvidence for genetic heterogeneity in X-linked congenital stationary night blindness.A new genetic locus for X linked progressive cone-rod dystrophyLinkage analysis of X-linked cone-rod dystrophy: localization to Xp11.4 and definition of a locus distinct from RP2 and RP3.Localization of a novel X-linked progressive cone dystrophy gene to Xq27: evidence for genetic heterogeneity.X-linked cone-rod dystrophy (locus COD1): identification of mutations in RPGR exon ORF15
P2860
Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1).
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1).
@ast
Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1).
@en
type
label
Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1).
@ast
Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1).
@en
prefLabel
Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1).
@ast
Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1).
@en
P2093
P2860
P1476
Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1)
@en
P2093
P2860
P304
P407
P577
1994-12-01T00:00:00Z