(Q51661004)

English

Detection by multiplex ligation-dependent probe amplification of large deletion mutations in the COL4A5 gene in female patients with Alport syndrome.

scientific article published on 24 January 2009

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/19169714

Detection by multiplex ligation-dependent probe amplification of large deletion mutations in the COL4A5 gene in female patients with Alport syndrome. (English)

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/19169714

Alport syndrome

1 reference

based on heuristic

inferred from title

author name string

Kandai Nozu

1

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/19169714

Rafal Przybyslaw Krol

2

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/19169714

Koichi Nakanishi

3

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/19169714

Norishige Yoshikawa

4

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/19169714

Yoshimi Nozu

5

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/19169714

Yasufumi Ohtsuka

6

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/19169714

Kazumoto Iijima

7

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/19169714

Masafumi Matsuo

8

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/19169714

publication date

24 January 2009

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/19169714

Pediatric Nephrology

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/19169714

24

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/19169714

9

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/19169714

1773-1774

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/19169714

https://scigraph.springernature.com/pub.10.1007/s00467-009-1122-0

0 references

Alport syndrome with diffuse leiomyomatosis. When and when not?

1 reference

https://api.crossref.org/works/10.1007%2FS00467-009-1122-0

21 January 2018

Alport syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19169714

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19169714

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analysis of patients with type III Bartter syndrome: picking up large heterozygous deletions with semiquantitative PCR

1 reference

https://pubmed.ncbi.nlm.nih.gov/19169714

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MLPA and cDNA analysis improves COL4A5 mutation detection in X-linked Alport syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19169714

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19169714

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Smooth muscle tumors associated with X-linked Alport syndrome: carrier detection in females

1 reference

https://pubmed.ncbi.nlm.nih.gov/19169714

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00467-009-1122-0

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/19169714

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 April 2018

http://europepmc.org/abstract/MED/19169714

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