Ocular phenotypes associated with biallelic mutations in BEST1 in Italian patients.
about
Restoration of mutant bestrophin-1 expression, localisation and function in a polarised epithelial cell modelScreening for BEST1 gene mutations in Chinese patients with bestrophinopathyBEST1 sequence variants in Italian patients with vitelliform macular dystrophyChoroidal neovascularization secondary to Best's vitelliform macular dystrophy in two siblings of a Malay family.Detailed analysis of family with autosomal recessive bestrophinopathy associated with new BEST1 mutation.
P2860
Ocular phenotypes associated with biallelic mutations in BEST1 in Italian patients.
description
2011 nî lūn-bûn
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2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Ocular phenotypes associated with biallelic mutations in BEST1 in Italian patients.
@ast
Ocular phenotypes associated with biallelic mutations in BEST1 in Italian patients.
@en
type
label
Ocular phenotypes associated with biallelic mutations in BEST1 in Italian patients.
@ast
Ocular phenotypes associated with biallelic mutations in BEST1 in Italian patients.
@en
prefLabel
Ocular phenotypes associated with biallelic mutations in BEST1 in Italian patients.
@ast
Ocular phenotypes associated with biallelic mutations in BEST1 in Italian patients.
@en
P2093
P2860
P1433
P1476
Ocular phenotypes associated with biallelic mutations in BEST1 in Italian patients
@en
P2093
Andrea Sodi
Francesca Menchini
Francesca Torricelli
Ilaria Passerini
Maria Pia Manitto
Ugo Menchini
Vittoria Murro
P2860
P304
P577
2011-11-24T00:00:00Z