A Heterozygous de novo Mutation in SLC41A1 Causes Hypomagnesemia and Renal Magnesium Wasting

Jeroen H.F. de Baaij; F. Arjona; Karl P Schlingmann; Stéphane Burtey; M. Thomassen; Jenny van Der Wijst; Nine Vam Knoers; René J.M. Bindels; Martin Konrad; Joost G.J. Hoenderop

Journal Articles FASEB Journal Year : 2017

A Heterozygous de novo Mutation in SLC41A1 Causes Hypomagnesemia and Renal Magnesium Wasting

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1

Jeroen H.F. de Baaij

Function : Author

F. Arjona

Function : Author

Karl P Schlingmann

Function : Author
PersonId : 873523

Stéphane Burtey

Function : Author
PersonId : 183685
IdHAL : stephane-burtey
IdRef : 111036372

Vascular research center of Marseille

M. Thomassen

Function : Author

Jenny van Der Wijst

Function : Author

Nine Vam Knoers

Function : Author

René J.M. Bindels

Function : Author
PersonId : 873517

Martin Konrad

Function : Author

Joost G.J. Hoenderop

Function : Author

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Life Sciences [q-bio]

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https://hal-amu.archives-ouvertes.fr/hal-01790063

Submitted on : Friday, May 11, 2018-4:05:56 PM

Last modification on : Wednesday, November 3, 2021-9:44:16 AM

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hal-01790063 , version 1 (11-05-2018)

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HAL Id : hal-01790063 , version 1

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Jeroen H.F. de Baaij, F. Arjona, Karl P Schlingmann, Stéphane Burtey, M. Thomassen, et al.. A Heterozygous de novo Mutation in SLC41A1 Causes Hypomagnesemia and Renal Magnesium Wasting. FASEB Journal, 2017. ⟨hal-01790063⟩

A Heterozygous de novo Mutation in SLC41A1 Causes Hypomagnesemia and Renal Magnesium Wasting

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