Identification of the human ortholog of the t-complex-encoded protein TCTE3 and evaluation as a candidate gene for primary ciliary dyskinesia.
about
A common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesiaGenetic analysis of the cytoplasmic dynein subunit families.Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 geneIdentification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patientsClinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome.Primary ciliary dyskinesia: clinical presentation, diagnosis and genetics.Management of primary ciliary dyskinesia/Kartagener's syndrome in infertile male patients and current progress in defining the underlying genetic mechanism.Identification of predicted human outer dynein arm genes: candidates for primary ciliary dyskinesia genes.T-complex-associated-testis-expressed 3 (TCTE3) is a novel marker for pancreatobiliary carcinomas.
P2860
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P2860
Identification of the human ortholog of the t-complex-encoded protein TCTE3 and evaluation as a candidate gene for primary ciliary dyskinesia.
description
2002 nî lūn-bûn
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name
Identification of the human or ...... or primary ciliary dyskinesia.
@en
Identification of the human or ...... or primary ciliary dyskinesia.
@nl
type
label
Identification of the human or ...... or primary ciliary dyskinesia.
@en
Identification of the human or ...... or primary ciliary dyskinesia.
@nl
prefLabel
Identification of the human or ...... or primary ciliary dyskinesia.
@en
Identification of the human or ...... or primary ciliary dyskinesia.
@nl
P2093
P356
P1476
Identification of the human or ...... or primary ciliary dyskinesia.
@en
P2093
J Konietzko
J Kreutzberger
J-D Drenckhahn
P Burfeind
P356
10.1159/000068545
P577
2002-01-01T00:00:00Z