(Q45272412)

11 December 2017

Phenotype and genotype of Dent's disease in three Korean boys (English)

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11 December 2017

Hae Il Cheong

1

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11 December 2017

Jung Won Lee

2

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11 December 2017

Shou Huan Zheng

3

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11 December 2017

Joo Hoon Lee

4

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11 December 2017

Ju Hyung Kang

5

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11 December 2017

Hee Gyung Kang

6

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11 December 2017

Il Soo Ha

7

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11 December 2017

Seung Joo Lee

8

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11 December 2017

Yong Choi

9

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11 December 2017

18 February 2005

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11 December 2017

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11 December 2017

20

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11 December 2017

4

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11 December 2017

455-459

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https://scigraph.springernature.com/pub.10.1007/s00467-004-1769-5

11 December 2017

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cites work

Chloride channel CLCN5 mutations in Japanese children with familial idiopathic low molecular weight proteinuria

1 reference

12 December 2020

Genetic mapping in the Xp11.2 region of a new form of X-linked hypophosphatemic rickets

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12 December 2020

X-linked recessive nephrolithiasis with renal failure

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12 December 2020

A common molecular basis for three inherited kidney stone diseases

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12 December 2020

Novel truncating mutations in the ClC-5 chloride channel gene in patients with Dent's disease

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12 December 2020

Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies

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12 December 2020

A new approach to mRNA in proximal tubule cells of patients with CLCN5 channelopathy

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12 December 2020

Dent's disease: can we slow its progression?

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12 December 2020

A second family with XLRH displays the mutation S244L in the CLCN5 gene

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12 December 2020

The clinical significance of asymptomatic low molecular weight proteinuria detected on routine screening of children in Japan: a survey of 53 patients

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12 December 2020

Hypercalciuria in children with hematuria

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12 December 2020

Pathogenesis of Dent's disease and related syndromes of X-linked nephrolithiasis

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12 December 2020

Clinical and genetic studies of CLCN5 mutations in Japanese families with Dent's disease

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12 December 2020

Responsiveness of hypercalciuria to thiazide in Dent's disease

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12 December 2020

Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5)

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12 December 2020

Evidence for genetic heterogeneity in Dent's disease

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12 December 2020

Mutations of CLCN5 in Japanese children with idiopathic low molecular weight proteinuria, hypercalciuria and nephrocalcinosis

1 reference

12 December 2020

Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.

1 reference

12 December 2020

X-linked hypercalciuric nephrolithiasis: clinical syndromes and chloride channel mutations

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12 December 2020

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12 December 2020

Hypercalciuria and nephrocalcinosis in patients with idiopathic low-molecular-weight proteinuria in Japan: is the disease identical to Dent's disease in United Kingdom?

1 reference

12 December 2020

Identification of two novel mutations in the CLCN5 gene in Japanese patients with familial idiopathic low molecular weight proteinuria (Japanese Dent's disease).

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12 December 2020

CLCN5 chloride-channel mutations in six new North American families with X-linked nephrolithiasis

1 reference

12 December 2020

10.1007/S00467-004-1769-5

Identifiers

DOI

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Dimensions Publication ID

11 December 2017

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1 reference