Comprehensive Analysis and Genetic Insights Into GJB2 c.35delG Mutation-Associated Non-Syndromic Hearing Loss in Morocco.

Salman EM, Qabli ME, Soufian L, Mansouri M, Bouzid FZ, Oulghoul O, Chehbouni M, Lakhdar Y, Rochdi Y, Raji A, Aboussair N

Open source

DOI
10.1002/oto2.70276
Published
2026 Jul-Sep
Container
OTO open
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.1002/oto2.70276,
  title = {Comprehensive Analysis and Genetic Insights Into GJB2 c.35delG Mutation-Associated Non-Syndromic Hearing Loss in Morocco.},
  author = {Salman EM and Qabli ME and Soufian L and Mansouri M and Bouzid FZ and Oulghoul O and Chehbouni M and Lakhdar Y and Rochdi Y and Raji A and Aboussair N},
  year = {2026},
  journal = {OTO open},
  doi = {10.1002/oto2.70276},
  url = {https://doi.org/10.1002/oto2.70276}
}

RIS

TY  - JOUR
TI  - Comprehensive Analysis and Genetic Insights Into GJB2 c.35delG Mutation-Associated Non-Syndromic Hearing Loss in Morocco.
AU  - Salman EM
AU  - Qabli ME
AU  - Soufian L
AU  - Mansouri M
AU  - Bouzid FZ
AU  - Oulghoul O
AU  - Chehbouni M
AU  - Lakhdar Y
AU  - Rochdi Y
AU  - Raji A
AU  - Aboussair N
PY  - 2026
JO  - OTO open
DO  - 10.1002/oto2.70276
UR  - https://doi.org/10.1002/oto2.70276
ER  - 

APA

EM, S., ME, Q., L, S., M, M., FZ, B., O, O., M, C., Y, L., Y, R., A, R., & N, A. (2026). Comprehensive Analysis and Genetic Insights Into GJB2 c.35delG Mutation-Associated Non-Syndromic Hearing Loss in Morocco.. OTO open. https://doi.org/10.1002/oto2.70276

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