Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish.
about
A CRISPR-based screen for Hedgehog signaling provides insights into ciliary function and ciliopathies.Whole exome sequencing reveals a mutation in ARMC9 as a cause of mental retardation, ptosis, and polydactyly.Zebrafish Models of Rare Hereditary Pediatric Diseases.Targeted disruption of the endogenous zebrafish locus as models of rapid rod photoreceptor degenerationMultiplexed CRISPR/Cas9 Targeting of Genes Implicated in Retinal Regeneration and Degeneration
P2860
Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish.
description
2017 nî lūn-bûn
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2017年の論文
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2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
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2017年论文
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2017年论文
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name
Mutations in ARMC9, which Enco ...... pathy Phenotypes in Zebrafish.
@en
type
label
Mutations in ARMC9, which Enco ...... pathy Phenotypes in Zebrafish.
@en
prefLabel
Mutations in ARMC9, which Enco ...... pathy Phenotypes in Zebrafish.
@en
P2093
P2860
P50
P1476
Mutations in ARMC9, which Enco ...... opathy Phenotypes in Zebrafish
@en
P2093
Arif O Khan
Brooke Latour
Dan Doherty
Deborah A Nickerson
Fowzan S Alkuraya
Himanshu Goel
Ian G Phelps
Jennifer C Dempsey
Julie C Van De Weghe
Matthias Gesemann
P2860
P356
10.1016/J.AJHG.2017.05.010
P407
P577
2017-06-15T00:00:00Z