CLDN19 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "CLDN19" in English language version.

Last modified: 04:56:14, 13 September 2026 (UTC)

Ref.Un. Ref.Website

Global rank English rank

5^th place

5^th place

630^th place

326^th place

2^nd place

2^nd place

doi.org (Global: 2^nd place; English: 2^nd place)

Naeem M, Hussain S, Akhtar N (2011). "Mutation in the tight-junction gene claudin 19 (CLDN19) and familial hypomagnesemia, hypercalciuria, nephrocalcinosis (FHHNC) and severe ocular disease". American Journal of Nephrology. 34 (3): 241–248. doi:10.1159/000330854. PMID 21791920.
Konrad M, Schaller A, Seelow D, Pandey AV, Waldegger S, Lesslauer A, et al. (November 2006). "Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement". American Journal of Human Genetics. 79 (5): 949–957. doi:10.1086/508617. PMC 1698561. PMID 17033971.

ensembl.org (Global: 630^th place; English: 326^th place)

may2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000164007 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000066058 – Ensembl, May 2017

nih.gov (Global: 5^th place; English: 5^th place)

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: CLDN19 claudin 19".
Konrad M, Schaller A, Seelow D, Pandey AV, Waldegger S, Lesslauer A, et al. (November 2006). "Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement". American Journal of Human Genetics. 79 (5): 949–957. doi:10.1086/508617. PMC 1698561. PMID 17033971.

pubmed.ncbi.nlm.nih.gov

Naeem M, Hussain S, Akhtar N (2011). "Mutation in the tight-junction gene claudin 19 (CLDN19) and familial hypomagnesemia, hypercalciuria, nephrocalcinosis (FHHNC) and severe ocular disease". American Journal of Nephrology. 34 (3): 241–248. doi:10.1159/000330854. PMID 21791920.
Konrad M, Schaller A, Seelow D, Pandey AV, Waldegger S, Lesslauer A, et al. (November 2006). "Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement". American Journal of Human Genetics. 79 (5): 949–957. doi:10.1086/508617. PMC 1698561. PMID 17033971.