Found: 3
Select item for more details and to access through your institution.
Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families.
- Published in:
- Biochemical Genetics, 2024, v. 62, n. 3, p. 1914, doi. 10.1007/s10528-023-10515-5
- By:
- Publication type:
- Article
Novel pathogenic WHRN variant causing hearing loss in a moroccan family.
- Published in:
- Molecular Biology Reports, 2023, v. 50, n. 12, p. 10663, doi. 10.1007/s11033-023-08901-8
- By:
- Publication type:
- Article
Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco.
- Published in:
- Molecular Biology Reports, 2022, v. 49, n. 5, p. 3949, doi. 10.1007/s11033-022-07245-z
- By:
- Publication type:
- Article