Identification of novel likely pathogenic variant in CDH23 causing non-syndromic hearing loss, and a novel variant in OTOGL in an extended Iranian family

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Identification of novel likely pathogenic variant in CDH23 causing non-syndromic hearing loss, and a novel variant in OTOGL in an extended Iranian family ; volume:25 ; number:1 ; day:14 ; month:9 ; year:2024 ; pages:1-8 ; date:12.2024
The Egyptian journal of medical human genetics ; 25, Heft 1 (14.9.2024), 1-8, 12.2024

Creator: Mohammadi, Aliasgar
Hoseinzadeh, Marziyeh
Narrei, Sina
Pourreza, Mohammad Reza
Mohammadi, Yousof
Norouzi, Mahnaz
Sadeghian, Ladan
Tabatabaiefar, Mohammad Amin

Contributor: SpringerLink (Online service)

DOI: 10.1186/s43042-024-00578-3

URN: urn:nbn:de:101:1-2411282106445.634284092270

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:23 AM CEST

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Mohammadi, Aliasgar
Hoseinzadeh, Marziyeh
Narrei, Sina
Pourreza, Mohammad Reza
Mohammadi, Yousof
Norouzi, Mahnaz
Sadeghian, Ladan
Tabatabaiefar, Mohammad Amin
SpringerLink (Online service)

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Identification of novel likely pathogenic variant in CDH23 causing non-syndromic hearing loss, and a novel variant in OTOGL in an extended Iranian family

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Other Objects (12)

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Splice-altering variant of PJVK gene in a Mauritanian family with non-syndromic hearing impairment

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