Mutation screening of Pakistani families with congenital eye disorders
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sameAs
Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan.Photoreceptor oxidative stress in hyperoxia-induced proliferative retinopathy accelerates rd8 degenerationThe role of crumbs genes in the vertebrate cornea.CRB1 mutations in inherited retinal dystrophiesThe molecular basis of retinal dystrophies in pakistan.Macular coloboma in siblings affected by different phenotypes of retinitis pigmentosa.MPP3 regulates levels of PALS1 and adhesion between photoreceptors and Müller cells.
P2860
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P2860
Mutation screening of Pakistani families with congenital eye disorders
description
2003 nî lūn-bûn
@nan
2003 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի մարտին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Mutation screening of Pakistani families with congenital eye disorders
@ast
Mutation screening of Pakistani families with congenital eye disorders
@en
Mutation screening of Pakistani families with congenital eye disorders
@nl
type
label
Mutation screening of Pakistani families with congenital eye disorders
@ast
Mutation screening of Pakistani families with congenital eye disorders
@en
Mutation screening of Pakistani families with congenital eye disorders
@nl
prefLabel
Mutation screening of Pakistani families with congenital eye disorders
@ast
Mutation screening of Pakistani families with congenital eye disorders
@en
Mutation screening of Pakistani families with congenital eye disorders
@nl
P2093
P1476
Mutation screening of Pakistani families with congenital eye disorders
@en
P2093
Abdul Hameed
Aisha Mohyuddin
Aiysha Abid
Khalid Anwar
Muhammad Ismail
S Qasim Mehdi
Shagufta Khaliq
Zobia Azmat
P356
10.1016/S0014-4835(02)00304-4
P407
P577
2003-03-01T00:00:00Z