MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss
- DOI
- 10.1086/323156
- Published
- 2001-09
- Container
- The American Journal of Human Genetics
- Publisher
- Elsevier BV
- Open access
- unknown
Credibility signals
uncertain Score 64/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
Show all credibility signals
- supportingDOI registered: A matching record was returned by Crossref.
- supportingDOI resolves: A matching record was returned by Crossref.
- not scoredDirectory of Open Access Journals: No matching DOAJ record was present in this response. No allow-list match; this is not evidence of low credibility.
- not scoredMEDLINE indexed: Not checked or no result supplied; no credibility inference made.
- not scoredOpenAlex core source: Not checked or no result supplied; no credibility inference made.
- not scoredKnown publisher allow-list: Not checked or no result supplied; no credibility inference made.
- not scoredROR affiliation: Not checked or no result supplied; no credibility inference made.
- not scoredRetraction Watch retraction: No retraction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch expression of concern: No expression of concern notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch correction: No correction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch reinstatement: No reinstatement notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredOpen access status: Not checked or no result supplied; no credibility inference made.
- not scoredPublication license: Not checked or no result supplied; no credibility inference made.
- not scoredPublication version: A publication version was supplied but is not scored.
- supportingMetadata completeness: All 6 scored descriptive metadata groups are present.
Cite this work
BibTeX
@article{allodium:10.1086/323156,
title = {MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss},
author = {Salvatore Melchionda and Nadav Ahituv and Luigi Bisceglia and Tama Sobe and Fabian Glaser and Raquel Rabionet and Maria Lourdes Arbones and Angelo Notarangelo and Enzo Di Iorio and Massimo Carella and Leopoldo Zelante and Xavier Estivill and Karen B. Avraham and Paolo Gasparini},
year = {2001},
journal = {The American Journal of Human Genetics},
doi = {10.1086/323156},
url = {https://doi.org/10.1086/323156}
}RIS
TY - JOUR TI - MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss AU - Salvatore Melchionda AU - Nadav Ahituv AU - Luigi Bisceglia AU - Tama Sobe AU - Fabian Glaser AU - Raquel Rabionet AU - Maria Lourdes Arbones AU - Angelo Notarangelo AU - Enzo Di Iorio AU - Massimo Carella AU - Leopoldo Zelante AU - Xavier Estivill AU - Karen B. Avraham AU - Paolo Gasparini PY - 2001 JO - The American Journal of Human Genetics DO - 10.1086/323156 UR - https://doi.org/10.1086/323156 ER -
APA
Melchionda, S., Ahituv, N., Bisceglia, L., Sobe, T., Glaser, F., Rabionet, R., Arbones, M. L., Notarangelo, A., Iorio, E. D., Carella, M., Zelante, L., Estivill, X., Avraham, K. B., & Gasparini, P. (2001). MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss. The American Journal of Human Genetics. https://doi.org/10.1086/323156
Source records
- crossref · retrieved 2026-09-27T12:37:06.728Z