Analysis of the T354P mutation of the sodium/iodide cotransporter gene in children with congenital hypothyroidism due to dyshormonogenesis.

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Analysis of the T354P mutation of the sodium/iodide cotransporter gene in children with congenital hypothyroidism due to dyshormonogenesis.

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2016 nî lūn-bûn

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2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

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name

Analysis of the T354P mutation ...... dism due to dyshormonogenesis.

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Analysis of the T354P mutation ...... dism due to dyshormonogenesis.

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prefLabel

Analysis of the T354P mutation ...... dism due to dyshormonogenesis.

@en

P1476

Analysis of the T354P mutation ...... dism due to dyshormonogenesis.

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P2093

Hajar Miranzadeh-Mahabadi

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Mahin Hashemipour

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Modjtaba Emadi-Baygi

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Neda Mostofizade

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Parvaneh Nikpour

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Silva Hovsepian

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P2860

Characterization of a novel loss of function mutation of PAX8 in a familial case of congenital hypothyroidism with in-place, normal-sized thyroid

Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia

Molecular analysis of the sodium/iodide symporter: impact on thyroid and extrathyroid pathophysiology

A novel mutation (Q40P) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia: evidence for phenotypic variability in mother and child

Congenital hypothyroidism caused by a mutation in the Na+/I- symporter

Expression, exon-intron organization, and chromosome mapping of the human sodium iodide symporter

Recurrent T354P mutation of the Na+/I- symporter in patients with iodide transport defect

Comparison of epidemiological data on congenital hypothyroidism in Europe with those of other parts in the world.

Congenital hypothyroidism.

Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: phenotypic variability and founder effect.

P304

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P31

scholarly article

P356

10.4103/2277-9175.180642

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P478

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P577

2016-04-19T00:00:00Z

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P698

27169104

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P921

birth defect

P932

4854026

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