Mutations in TBL1X Are Associated With Central Hypothyroidism.
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Pediatric Hypothyroidism: Diagnosis and Treatment.The actions of thyroid hormone signaling in the nucleus.Central hypothyroidism - a neglected thyroid disorder.Congenital Central Hypothyroidism Caused by a Novel Thyroid-Stimulating Hormone-Beta Subunit Gene Mutation in Two Siblings.Congenital hypothyroidism: insights into pathogenesis and treatment.TRH Action Is Impaired in Pituitaries of Male IGSF1-Deficient Mice.NCoR1-independent mechanism plays a role in the action of the unliganded thyroid hormone receptor.Pilot Neonatal Screening Program for Central Congenital Hypothyroidism: Evidence of Significant Detection.Central Hypothyroidism Due to a TRHR Mutation Causing Impaired Ligand Affinity and Transactivation of Gq.A heritable microduplication encompassing TBL1XR1 causes a genomic sister-disorder for the 3q26.32 microdeletion syndrome.Two siblings with congenital central hypothyroidism caused by a novel mutation in the IGSF1 gene.2018 European Thyroid Association (ETA) Guidelines on the Diagnosis and Management of Central Hypothyroidism
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Mutations in TBL1X Are Associated With Central Hypothyroidism.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 07 September 2016
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Mutations in TBL1X Are Associated With Central Hypothyroidism.
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Mutations in TBL1X Are Associated With Central Hypothyroidism.
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type
label
Mutations in TBL1X Are Associated With Central Hypothyroidism.
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Mutations in TBL1X Are Associated With Central Hypothyroidism.
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prefLabel
Mutations in TBL1X Are Associated With Central Hypothyroidism.
@en
Mutations in TBL1X Are Associated With Central Hypothyroidism.
@nl
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P2860
P50
P356
P1476
Mutations in TBL1X Are Associated With Central Hypothyroidism
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A S Paul van Trotsenburg
Anita Boelen
Charlotte A Heinen
Eric Fliers
Erica L T van den Akker
Gijs W E Santen
Mariëlle Alders
Monique Losekoot
Nienke R Biermasz
P2860
P304
P356
10.1210/JC.2016-2531
P407
P577
2016-09-07T00:00:00Z