A Heterozygous de novo Mutation in SLC41A1 Causes Hypomagnesemia and Renal Magnesium Wasting - Aix-Marseille Université Access content directly
Journal Articles FASEB Journal Year : 2017

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

Jeroen H.F. de Baaij
  • Function : Author
F. Arjona
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Karl P Schlingmann
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  • PersonId : 873523
Stéphane Burtey
M. Thomassen
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Jenny van Der Wijst
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Nine Vam Knoers
  • Function : Author
René J.M. Bindels
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  • PersonId : 873517
Martin Konrad
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Joost G.J. Hoenderop
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Dates and versions

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⟩

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