about
Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypesCo-activator candidate interactions for orphan nuclear receptor NR2E1.The Orphan Nuclear Receptor TLX/NR2E1 in Neural Stem Cells and Diseases.Functional characterization of zebrafish orthologs of the human Beta 3-Glucosyltransferase B3GLCT gene mutated in Peters Plus Syndrome.
P2860
description
2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
@wuu
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh
2012年學術文章
@zh-hant
name
Absence of NR2E1 mutations in patients with aniridia.
@ast
Absence of NR2E1 mutations in patients with aniridia.
@en
type
label
Absence of NR2E1 mutations in patients with aniridia.
@ast
Absence of NR2E1 mutations in patients with aniridia.
@en
prefLabel
Absence of NR2E1 mutations in patients with aniridia.
@ast
Absence of NR2E1 mutations in patients with aniridia.
@en
P2093
P2860
P50
P1433
P1476
Absence of NR2E1 mutations in patients with aniridia
@en
P2093
Angela Brooks-Wilson
Brian P Brooks
Francesca Pasutto
Hanne Jensen
Ian M Macdonald
Johanna M Schuetz
Michael A Walter
Thomas Rosenberg
Ximena Corso-Díaz
P2860
P304
P577
2012-11-22T00:00:00Z