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35433171 | Sodium-glucose cotransporter type 2 channel inhibitor: Breakthrough in the treatment of neutropenia in patients with glycogen storage disease type 1b? | 2022 May |
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33964207 | A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction. | 2021 Jun 3 |
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2 |
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1 |
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2 |
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2 |
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1 |
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1 |
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1 |
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1 |
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2 |