Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia. (Q55058934)

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2 March 2020

title

Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia (English)

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2 March 2020

1

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2 March 2020

author name string

Eiske M Dorresteijn

2

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2 March 2020

Eric A M Hennekam

3

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2 March 2020

Erik-Jan Kamsteeg

4

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2 March 2020

Rowdy Meijer

5

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2 March 2020

Karin Dahan

6

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2 March 2020

Michelle Muller

7

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2 March 2020

Marinus A van den Dorpel

8

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2 March 2020

René J M Bindels

9

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2 March 2020

Joost G J Hoenderop

10

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2 March 2020

Olivier Devuyst

11

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2 March 2020

Nine V A M Knoers

12

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2 March 2020

language of work or name

English

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publication date

11 March 2015

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Nephrology Dialysis Transplantation

2 March 2020

published in

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2 March 2020

volume

30

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2 March 2020

page(s)

952-957

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2 March 2020

issue

6

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Drug-induced alterations in Mg2+ homoeostasis

2 March 2020

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Hereditary isolated renal magnesium loss maps to chromosome 11q23.

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Renal magnesium wasting in two families with autosomal dominant inheritance

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FXYD proteins stabilize Na,K-ATPase: amplification of specific phosphatidylserine-protein interactions

21 January 2018

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Splice variants of the gamma subunit (FXYD2) and their significance in regulation of the Na, K-ATPase in kidney

21 January 2018

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Distribution and oligomeric association of splice forms of Na(+)-K(+)-ATPase regulatory gamma-subunit in rat kidney

21 January 2018

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HNF1B mutations associate with hypomagnesemia and renal magnesium wasting

21 January 2018

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HNF-1B specifically regulates the transcription of the γa-subunit of the Na+/K+-ATPase

21 January 2018

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Mutations in PCBD1 cause hypomagnesemia and renal magnesium wasting.

21 January 2018

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Magnesium modulates ROMK channel-mediated potassium secretion

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Mechanism of hypokalemia in magnesium deficiency.

21 January 2018

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Transcriptional and functional analyses of SLC12A3 mutations: new clues for the pathogenesis of Gitelman syndrome.

21 January 2018

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