Compound Heterozygosity for OTOA Truncating Variant and Genomic Rearrangement Cause Autosomal Recessive Sensorineural Hearing Loss in an Italian Family.
- DOI
- 10.3390/audiolres11030041
- Published
- 2021 Sep 9
- Container
- Audiology research
- Publisher
- Not recorded
- Open access
- yes
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BibTeX
@article{allodium:10.3390/audiolres11030041,
title = {Compound Heterozygosity for OTOA Truncating Variant and Genomic Rearrangement Cause Autosomal Recessive Sensorineural Hearing Loss in an Italian Family.},
author = {Ortore RP and Leone MP and Palumbo O and Petracca A and Trecca EMC and D'Ecclesia A and Vigliaroli CL and Micale L and Longo F and Melchionda S and Castori M},
year = {2021},
journal = {Audiology research},
doi = {10.3390/audiolres11030041},
url = {https://doi.org/10.3390/audiolres11030041}
}RIS
TY - JOUR TI - Compound Heterozygosity for OTOA Truncating Variant and Genomic Rearrangement Cause Autosomal Recessive Sensorineural Hearing Loss in an Italian Family. AU - Ortore RP AU - Leone MP AU - Palumbo O AU - Petracca A AU - Trecca EMC AU - D'Ecclesia A AU - Vigliaroli CL AU - Micale L AU - Longo F AU - Melchionda S AU - Castori M PY - 2021 JO - Audiology research DO - 10.3390/audiolres11030041 UR - https://doi.org/10.3390/audiolres11030041 ER -
APA
RP, O., MP, L., O, P., A, P., EMC, T., A, D., CL, V., L, M., F, L., S, M., & M, C. (2021). Compound Heterozygosity for OTOA Truncating Variant and Genomic Rearrangement Cause Autosomal Recessive Sensorineural Hearing Loss in an Italian Family.. Audiology research. https://doi.org/10.3390/audiolres11030041
Source records
- pubmed · retrieved 2026-09-26T13:08:43.278Z