A nonsense mutation in CEP55 defines a new locus for a Meckel-like syndrome, an autosomal recessive lethal fetal ciliopathy.
about
Regulation of cytokinesis during corticogenesis: focus on the midbody.Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes.Meckel-Gruber Syndrome: An Update on Diagnosis, Clinical Management, and Research Advances.CEP55 is a determinant of cell fate during perturbed mitosis in breast cancer
P2860
A nonsense mutation in CEP55 defines a new locus for a Meckel-like syndrome, an autosomal recessive lethal fetal ciliopathy.
description
2017 nî lūn-bûn
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name
A nonsense mutation in CEP55 d ...... ssive lethal fetal ciliopathy.
@en
A nonsense mutation in CEP55 d ...... ssive lethal fetal ciliopathy.
@nl
type
label
A nonsense mutation in CEP55 d ...... ssive lethal fetal ciliopathy.
@en
A nonsense mutation in CEP55 d ...... ssive lethal fetal ciliopathy.
@nl
prefLabel
A nonsense mutation in CEP55 d ...... ssive lethal fetal ciliopathy.
@en
A nonsense mutation in CEP55 d ...... ssive lethal fetal ciliopathy.
@nl
P2093
P2860
P50
P356
P1433
P1476
A nonsense mutation in CEP55 d ...... essive lethal fetal ciliopathy
@en
P2093
C Frykholm
J Wesström
M-L Bondeson
P2860
P304
P356
10.1111/CGE.13012
P577
2017-05-03T00:00:00Z