(Q41919908)

14 October 2017

title

X-linked MCT8 gene mutations: characterization of the pediatric neurologic phenotype (English)

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14 October 2017

Kenton R Holden

1

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14 October 2017

Oscar F Zuñiga

2

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14 October 2017

Melanie M May

3

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14 October 2017

Humberto Su

4

1 reference

14 October 2017

Marco R Molinero

5

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14 October 2017

R Curtis Rogers

6

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14 October 2017

Charles E Schwartz

7

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14 October 2017

publication date

1 October 2005

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Journal of Child Neurology

14 October 2017

published in

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14 October 2017

volume

20

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14 October 2017

issue

10

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14 October 2017

page(s)

852-857

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Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene

14 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200101601

A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200101601

Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200101601

X-linked paroxysmal dyskinesia and severe global retardation caused by defective MCT8 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738050200101601

10.1177/08830738050200101601

21 January 2018

Identifiers

DOI

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14 October 2017

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