A human laterality disorder associated with recessive CCDC11 mutation.
about
A human laterality disorder caused by a homozygous deleterious mutation in MMP21A Zebrafish Loss-of-Function Model for Human CFAP53 Mutations Reveals Its Specific Role in Laterality Organ FunctionThe determination factors of left-right asymmetry disorders- a short review.Common bile duct adenocarcinoma in a patient with situs inversus totalis: report of a rare caseA human laterality disorder associated with a homozygous WDR16 deletion.Ccdc11 is a novel centriolar satellite protein essential for ciliogenesis and establishment of left-right asymmetry.Genetic basis of human left-right asymmetry disorders.Hairy cell leukemia in a patient with situs inversus totalis: an extremely rare combination.Rare novel variants in the ZIC3 gene cause X-linked heterotaxy.Mutations in CCDC11, which encodes a coiled-coil containing ciliary protein, causes situs inversus due to dysmotility of monocilia in the left-right organizer.Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility
P2860
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P2860
A human laterality disorder associated with recessive CCDC11 mutation.
description
2012 nî lūn-bûn
@nan
2012 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
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name
A human laterality disorder associated with recessive CCDC11 mutation.
@ast
A human laterality disorder associated with recessive CCDC11 mutation.
@en
A human laterality disorder associated with recessive CCDC11 mutation.
@nl
type
label
A human laterality disorder associated with recessive CCDC11 mutation.
@ast
A human laterality disorder associated with recessive CCDC11 mutation.
@en
A human laterality disorder associated with recessive CCDC11 mutation.
@nl
prefLabel
A human laterality disorder associated with recessive CCDC11 mutation.
@ast
A human laterality disorder associated with recessive CCDC11 mutation.
@en
A human laterality disorder associated with recessive CCDC11 mutation.
@nl
P2093
P1476
A human laterality disorder associated with recessive CCDC11 mutation.
@en
P2093
Asaf Ta-Shma
Avraham Shaag
Azaria J J T Rein
Orly Elpeleg
Tom Einbinder
Yuval Cinnamon
Zeev Perles
P304
P356
10.1136/JMEDGENET-2011-100457
P407
P577
2012-05-10T00:00:00Z