(Q28239740)

English

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

scientific article (publication date: June 1997)

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title

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

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main subject

congenital disorder

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congenital hypothyroidism

1 reference

H Fujiwara

1

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K Tatsumi

series ordinal

2

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K Miki

series ordinal

3

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T Harada

series ordinal

4

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K Miyai

series ordinal

5

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S Takai

series ordinal

6

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N Amino

series ordinal

7

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language of work or name

English

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publication date

June 1997

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published in

Nature Genetics

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volume

16

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page(s)

124-5

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issue

2

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exact match

https://scigraph.springernature.com/pub.10.1038/ng0697-124

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cites work

Cloning and characterization of the thyroid iodide transporter

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG0697-124

retrieved

21 April 2017

Cloning of the human sodium lodide symporter

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG0697-124

retrieved

21 April 2017

Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/NG0697-124

retrieved

21 April 2017

A functional superfamily of sodium/solute symporters

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0697-124

retrieved

21 January 2018

The syndromes of resistance to thyroid hormone

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0697-124

retrieved

21 January 2018

Congenital Goiter with Defective Iodide Transport

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0697-124

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Cretinism with combined hormone deficiency caused by a mutation in the PIT1 gene

1 reference

stated in

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reference URL

https://api.crossref.org/works/10.1038%2FNG0697-124

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A 3' splice site mutation in the thyroglobulin gene responsible for congenital goiter with hypothyroidism

1 reference

stated in

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reference URL

https://api.crossref.org/works/10.1038%2FNG0697-124

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goiter

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0697-124

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Iodide transport in a continuous line of cultured cells from rat thyroid

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0697-124

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

(Q28239740)

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

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