PCDH15 (Spanish Wikipedia)

Analysis of information sources in references of the Wikipedia article "PCDH15" in Spanish language version.

Last modified: 04:17:01, 20 December 2025 (UTC)

Ref.Un. Ref.Website

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11adsabs.harvard.edu

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adsabs.harvard.edu (Global: 14^th place; Spanish: 43^rd place)

«Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells». Nature 449 (7158): 87-91. September 2007. Bibcode:2007Natur.449...87K. PMID 17805295. doi:10.1038/nature06091.

archive.org (Global: 6^th place; Spanish: 4^th place)

«Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F». American Journal of Human Genetics 69 (1): 25-34. July 2001. PMC 1226045. PMID 11398101. doi:10.1086/321277.
«Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells». Nature 449 (7158): 87-91. September 2007. Bibcode:2007Natur.449...87K. PMID 17805295. doi:10.1038/nature06091.

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

dx.doi.org

«Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F». American Journal of Human Genetics 69 (1): 25-34. July 2001. PMC 1226045. PMID 11398101. doi:10.1086/321277.
«PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23». Human Molecular Genetics 12 (24): 3215-23. December 2003. PMID 14570705. doi:10.1093/hmg/ddg358.
«Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells». Nature 449 (7158): 87-91. September 2007. Bibcode:2007Natur.449...87K. PMID 17805295. doi:10.1038/nature06091.
«Genetics of the human face: Identification of large-effect single gene variants». Proceedings of the National Academy of Sciences of the United States of America 115 (4): E676-E685. January 2018. PMC 5789906. PMID 29301965. doi:10.1073/pnas.1708207114.

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

ncbi.nlm.nih.gov

«Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F». American Journal of Human Genetics 69 (1): 25-34. July 2001. PMC 1226045. PMID 11398101. doi:10.1086/321277.
«PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23». Human Molecular Genetics 12 (24): 3215-23. December 2003. PMID 14570705. doi:10.1093/hmg/ddg358.
«Entrez Gene: PCDH15 protocadherin 15».
«Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells». Nature 449 (7158): 87-91. September 2007. Bibcode:2007Natur.449...87K. PMID 17805295. doi:10.1038/nature06091.
«Genetics of the human face: Identification of large-effect single gene variants». Proceedings of the National Academy of Sciences of the United States of America 115 (4): E676-E685. January 2018. PMC 5789906. PMID 29301965. doi:10.1073/pnas.1708207114.