(Q47301048)

13 January 2018

title

Mutations in the CLCN5 gene in Japanese patients with familial idiopathic low-molecular-weight proteinuria (English)

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13 January 2018

author name string

Nakazato H

1

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13 January 2018

Hattori S

2

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13 January 2018

Furuse A

3

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13 January 2018

Kawano T

4

1 reference

13 January 2018

Karashima S

5

1 reference

13 January 2018

Tsuruta M

6

1 reference

13 January 2018

Yoshimuta J

7

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13 January 2018

Endo F

8

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13 January 2018

Matsuda I

9

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13 January 2018

language of work or name

English

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publication date

1 October 1997

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13 January 2018

published in

Kidney International

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13 January 2018

volume

52

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13 January 2018

issue

4

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13 January 2018

page(s)

895-900

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13 January 2018

https://scigraph.springernature.com/pub.10.1038/ki.1997.410

exact match

0 references

cites work

X-linked recessive nephrolithiasis with renal failure

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.410

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.410

7 January 2021

Cloning and characterization of CLCN5, the human kidney chloride channel gene implicated in Dent disease (an X-linked hereditary nephrolithiasis)

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.410

7 January 2021

A common molecular basis for three inherited kidney stone diseases

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.410

7 January 2021

Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.410

7 January 2021

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.410

7 January 2021

Identification of a single base insertion in the COL4A5 gene in Alport syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.410

7 January 2021

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.410

7 January 2021

Specificity of PCR-SSCP for detection of the mutant ornithine transcarbamylase (OTC) gene in patients with OTC deficiency

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.410

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.1997.410

7 January 2021

Identifiers

DOI

10.1038/KI.1997.410

1 reference

13 January 2018

1 reference

13 January 2018