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Dergiler / Cukurova Medical Journal / 2018 / Cilt: 43 - Sayı: 4

Konjenital glukoz galaktoz malabsorbsiyonu sendromunda yeni bir mutasyon

A novel mutation in congenital glucose galactose malabsorption syndrome

Mehmet Satar
Mustafa Akçalı
Hacer Yapıcıoğlu Yıldızdaş
Ferda Özlü
Mehmet Ağın
Gökhan Tümgör
Atıl Bişgin
Sayfa
1062–1064
Yayın Tarihi
2018-12-29
DOI
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Özet

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Abstract

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Bu Makaleye Atıf Yap

Satar, M., Akçalı, M., Yıldızdaş, H. Y., Özlü, F., Ağın, M., Tümgör, G., Bişgin, A. (2018). Konjenital glukoz galaktoz malabsorbsiyonu sendromunda yeni bir mutasyon. Cukurova Medical Journal, Cilt: 43 - Sayı: 4, 1062–1064. https://ajindex.com/articles/121126

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Kaynakça (12)

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  9. Soylu OB, Ecevit C, Altinöz S et al. Nephrocalcinosis in glucose-galactose malabsorption: nephrocalcinosis and proximal tubular dysfunction in a young infant with a novel mutation of SGLT1. Eur J Pediatr. 2008;167:1395-8
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