(Q50335672)

5 March 2018

title

Dual degradation mechanisms ensure disposal of NHE6 mutant protein associated with neurological disease. (English)

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5 March 2018

5

Harald Stenmark

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5 March 2018

Ingrid Roxrud

1

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5 March 2018

Camilla Raiborg

series ordinal

2

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5 March 2018

Gregor D Gilfillan

series ordinal

3

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5 March 2018

Petter Strømme

series ordinal

4

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5 March 2018

language of work or name

English

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publication date

17 July 2009

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5 March 2018

Experimental Cell Research

published in

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5 March 2018

volume

315

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5 March 2018

issue

17

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5 March 2018

page(s)

3014-3027

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5 March 2018

Angelman syndrome: a review of the clinical and genetic aspects

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SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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X linked severe mental retardation, craniofacial dysmorphology, epilepsy, ophthalmoplegia, and cerebellar atrophy in a large South African kindred is localised to Xq24-q27.

7 January 2021

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10.1016/J.YEXCR.2009.07.012

7 January 2021

Identifiers

DOI

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5 March 2018

release_553ybtetubcqjnqgme2e4dp27e

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/553ybtetubcqjnqgme2e4dp27e

mapped directly with Wikidata item

24 November 2022

based on heuristic

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5 March 2018