A family with novel homozygous deletion mutation(c.1255delT; p.Phe419Serfs*12) in the glucokinasegene, which is a rare cause of permanent neonataldiabetes mellitus için istatistikler
Toplam ziyaret
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| A family with novel homozygous deletion mutation(c.1255delT; p.Phe419Serfs*12) in the glucokinasegene, which is a rare cause of permanent neonataldiabetes mellitus | 1 |
Aylık toplam ziyaret
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| Mayıs 2026 | 0 |
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| Temmuz 2026 | 0 |
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| Kasım 2026 | 0 |
Dosya Ziyaretleri
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| 12530.pdf | 37 |
