Molecular spectrum of TSHβ subunit gene defects in central hypothyroidism in the UK and Ireland

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Pediatric Hypothyroidism: Diagnosis and Treatment.Central hypothyroidism - a neglected thyroid disorder.Congenital hypothyroidism: insights into pathogenesis and treatment.Pilot Neonatal Screening Program for Central Congenital Hypothyroidism: Evidence of Significant Detection.

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P2860

Molecular spectrum of TSHβ subunit gene defects in central hypothyroidism in the UK and Ireland

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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 30 June 2016

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vedecký článok

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videnskabelig artikel

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vědecký článek

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Molecular spectrum of TSHβ sub ...... yroidism in the UK and Ireland

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Molecular spectrum of TSHβ sub ...... roidism in the UK and Ireland.

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Molecular spectrum of TSHβ sub ...... yroidism in the UK and Ireland

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Molecular spectrum of TSHβ sub ...... roidism in the UK and Ireland.

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Molecular spectrum of TSHβ sub ...... yroidism in the UK and Ireland

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Molecular spectrum of TSHβ sub ...... roidism in the UK and Ireland.

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P1476

Molecular spectrum of TSHβ sub ...... yroidism in the UK and Ireland

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A K Nicholas

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B Bernhard

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E Crowne

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E Schoenmakers

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G Lyons

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J Kirk

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M T Dattani

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N Schoenmakers

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S Jaleel

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V K Chatterjee

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P2860

Thyroid-stimulating hormone (TSH) deficiency caused by a single base substitution in the CAGYC region of the beta-subunit

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Thyroid hormone receptor beta-dependent expression of a potassium conductance in inner hair cells at the onset of hearing.

An evo-devo approach to thyroid hormones in cerebral and cerebellar cortical development: etiological implications for autism

SignalP 4.0: discriminating signal peptides from transmembrane regions

Hyperplastic pituitary gland, high serum glycoprotein hormone alpha-subunit, and variable circulating thyrotropin (TSH) levels as hallmark of central hypothyroidism due to mutations of the TSH beta gene.

New autosomal recessive mutation of the TSH-beta subunit gene causing central isolated hypothyroidism.

Congenital central hypothyroidism due to homozygous thyrotropin beta 313 Delta T mutation is caused by a Founder effect.

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10.1111/CEN.13149

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Edna Roche

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Molecular spectrum of TSHβ subunit gene defects in central hypothyroidism in the UK and Ireland

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P2860

P2860

Molecular spectrum of TSHβ subunit gene defects in central hypothyroidism in the UK and Ireland

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P1433

P1476

P2093

P2860

P304

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P433

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P698

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P1433

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P2093

P2860

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P478

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P698

P932