LE WE PMID CA
Dent s syndrome646Dent Syndrom

Bartter s syndrome

Calcium (Hypercalciuria)

CASR

CLC Kb

ClC5

CLCN5

Dent s syndrome

Hypercalciuric nephrolithiasis with hypophosphatemia

Hypocalciemic hypercalciuria autosomal dominant

Hypomagnesemia with hypercalciuria familiar

Kidney (Malformation)

Lowe s syndrome

Nephrocalcinosis

NPT2c

OCRL1

Paracellin1

Phosphatidlyinositol 4 5 bisphosphate 5 phosphatase

TRPV6

2000  
1
Pathogenesis of Dent's disease and related syndromes of X-linked nephrolithiasis.
[10720930] Kidney Int 57(3): 787-93 (2000)
1998  
2
X-linked hypercalciuric nephrolithiasis: clinical syndromes and chloride channel mutations.
[9452994] Kidney Int 53(1): 3-17 (1998)
2006  
3
Recent advances in understanding the clinical and genetic heterogeneity of Dent's disease.
[16861240] Nephrol Dial Transplant 21(10): 2708-17 (2006)
2009  
4
Genetic causes of hypercalciuric nephrolithiasis.
[18446382] Pediatr Nephrol 24(12): 2321-32 (2009)
2010  
5
2012  
6
Suppression of intestinal calcium entry channel TRPV6 by OCRL, a lipid phosphatase associated with Lowe syndrome and Dent disease.
[22378746] Am J Physiol Cell Physiol 302(10): C1479-91 (2012)
2009  
7
Hypophosphatemic rickets due to Dent's disease: A case report and review of literature.
[20535254] Indian J Nephrol 19(4): 163-6 (2009)

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