edoc

A new nonsense mutation in; HMX1; in two siblings with oculoauricular syndrome

Ansar, Muhammad and Javed, Samra and Baig, Hafiz Muhammad Azhar and Quinodoz, Mathieu and Ullah, Mukhtar and Han, Ji Hoon and Rahim, Muhammad Usama and Kausar, Humera and Calzetti, Giacomo and Rivolta, Carlo. (2022) A new nonsense mutation in; HMX1; in two siblings with oculoauricular syndrome. Ophthalmic Genetics, 43 (5). pp. 720-723.

[img] PDF - Published Version
Available under License CC BY-NC-ND (Attribution-NonCommercial-NoDerivatives).

2210Kb

Official URL: https://edoc.unibas.ch/95555/

Downloads: Statistics Overview


Faculties and Departments:03 Faculty of Medicine > Bereich Spezialfächer (Klinik) > Ophthalmologie USB
03 Faculty of Medicine > Departement Klinische Forschung > Bereich Spezialfächer (Klinik) > Ophthalmologie USB
09 Associated Institutions > Institute of Molecular and Clinical Ophthalmology Basel (IOB) > Research Group Rivolta IOB
UniBasel Contributors:Rivolta, Carlo
Item Type:Article, refereed
Article Subtype:Further Journal Contribution
Publisher:Taylor & Francis Group
ISSN:1381-6810
e-ISSN:1744-5094
Note:Publication type according to Uni Basel Research Database: Journal item
Language:English
Related URLs:
Identification Number:
edoc DOI:
Last Modified:20 Sep 2023 08:12
Deposited On:20 Sep 2023 08:12

Repository Staff Only: item control page