Mutation of serine/threonine protein kinase 36 (STK36) causes primary ciliary dyskinesia with a central pair defect.
about
An effective combination of whole-exome sequencing and runs of homozygosity for the diagnosis of primary ciliary dyskinesia in consanguineous families.Motile cilia defects in diseases other than primary ciliary dyskinesia: The contemporary diagnostic and research role for transmission electron microscopy.Airway ciliary dysfunction and respiratory symptoms in patients with transposition of the great arteries.Primary ciliary dyskinesia: keep it on your radar.
P2860
Mutation of serine/threonine protein kinase 36 (STK36) causes primary ciliary dyskinesia with a central pair defect.
description
2017 nî lūn-bûn
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2017年の論文
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2017年論文
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2017年論文
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2017年論文
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2017年論文
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2017年論文
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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
Mutation of serine/threonine p ...... ia with a central pair defect.
@en
type
label
Mutation of serine/threonine p ...... ia with a central pair defect.
@en
prefLabel
Mutation of serine/threonine p ...... ia with a central pair defect.
@en
P2093
P2860
P356
P1433
P1476
Mutation of serine/threonine p ...... ia with a central pair defect.
@en
P2093
Christine Edelbusch
Gerard W Dougherty
Israel Amirav
Joseph Rivlin
Julia Wallmeier
Niki T Loges
Petra Pennekamp
Sandra Cindrić
P2860
P304
P356
10.1002/HUMU.23261
P577
2017-05-23T00:00:00Z