solute carrier family 37 (glycerol-6-phosphate transporter), member 4, - Protein

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Treatment recommendations for glycogen storage disease type IB- associated neutropenia and neutrophil dysfunction with empagliflozin: Consensus from an international workshop. [Mol Genet Metab. 2024]
Treatment recommendations for glycogen storage disease type IB- associated neutropenia and neutrophil dysfunction with empagliflozin: Consensus from an international workshop.
Grünert SC, Derks TGJ, Mundy H, Dalton RN, Donadieu J, Hofbauer P, Jones N, Uçar SK, LaFreniere J, Contreras EL, et al. Mol Genet Metab. 2024 Mar; 141(3):108144. Epub 2024 Jan 17.
Three novel SLC37A4 variants in glycogen storage disease type 1b and a literature review. [J Int Med Res. 2023]
Three novel SLC37A4 variants in glycogen storage disease type 1b and a literature review.
Wang Z, Zhao R, Jia X, Li X, Ma L, Fu H. J Int Med Res. 2023 Dec; 51(12):3000605231216633.
A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction. [Am J Hum Genet. 2021]
A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction.
Ng BG, Sosicka P, Fenaille F, Harroche A, Vuillaumier-Barrot S, Porterfield M, Xia ZJ, Wagner S, Bamshad MJ, Vergnes-Boiteux MC, et al. Am J Hum Genet. 2021 Jun 3; 108(6):1040-1052. Epub 2021 May 7.

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glucose-6-phosphate exchanger SLC37A4 isoform 1 [Homo sapiens]
glucose-6-phosphate exchanger SLC37A4 isoform 1 [Homo sapiens]
gi|256219483|ref|NP_001157749.1|

Protein
Chain B, HPV E7 peptide
Chain B, HPV E7 peptide
gi|848130481|pdb|4YOZ|B

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