A heterozygous c-Maf transactivation domain mutation causes congenital cataract and enhances target gene activation.
about
Structural Basis of Alternative DNA Recognition by Maf Transcription FactorsMutations Impairing GSK3-Mediated MAF Phosphorylation Cause Cataract, Deafness, Intellectual Disability, Seizures, and a Down Syndrome-like Facies.Chromosomal rearrangements and novel genes in disorders of eye development, cataract and glaucoma.Mutation update of transcription factor genes FOXE3, HSF4, MAF, and PITX3 causing cataracts and other developmental ocular defects.
P2860
A heterozygous c-Maf transactivation domain mutation causes congenital cataract and enhances target gene activation.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
A heterozygous c-Maf transacti ...... hances target gene activation.
@en
type
label
A heterozygous c-Maf transacti ...... hances target gene activation.
@en
prefLabel
A heterozygous c-Maf transacti ...... hances target gene activation.
@en
P2093
P2860
P356
P1476
A heterozygous c-Maf transacti ...... hances target gene activation.
@en
P2093
P2860
P304
P356
10.1093/HMG/DDM048
P50
P577
2007-03-20T00:00:00Z