Dergiler / Türk Pediatri Arşivi / 2013 / Cilt: 48 - Sayı: 4

Nefrolityazis tanısıyla başvuran bir olguda Dent hastalığı

Dent’s disease in a child with nephrolithiasis

Sayfa
347–349
Yayın Tarihi
2022-11-05
DOI
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Bu Makaleye Atıf Yap

GÖKÇE, İ., DENİZ, N. Ç., YILDIZ, N., ALTUNTAŞ, Ü., ALPAY, H. (2022). Nefrolityazis tanısıyla başvuran bir olguda Dent hastalığı. Türk Pediatri Arşivi, Cilt: 48 - Sayı: 4, 347–349. https://ajindex.com/articles/641302

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Kaynakça (13)

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  10. Hoopes RR Jr, Shrimpton AE, Knohl SJ, et al. Dent disease with mutations in OCRL1. Am J Hum Genet 2005; 76: 260-7
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  12. Tosetto E, Ghiggeri GM, Emma F et al. Phenotypic and genetic heterogeneity in Dent’s disease--the results of an Italian collaborative study. Nephrol Dial Transplant 2006; 21: 2452-63
  13. Reinhart SC, Norden AG, Lapsley M, et al. Characterization of carrier females and affected males with X-linked recessive nephrolithiasis. J Am Soc Nephrol 1995; 5: 1451-61.