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Wiley, Human Mutation: Variation, Informatics and Disease, 10(42), p. 1321-1335, 2021

DOI: 10.1002/humu.24260

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Variants of human CLDN9 cause mild to profound hearing loss

Journal article published in 2021 by Memoona Ramzan ORCID, Oumaima Zarrik ORCID, Christophe Philippe ORCID, Cristina Fenollar‐Ferrer ORCID, Inna A. Belyantseva ORCID, Yoko Nakano ORCID, Risa Tona ORCID, Zunaira Munir ORCID, Rizwan Yousaf ORCID, Hafiza Idrees ORCID, Midhat Salman ORCID, Rasheeda Basheer ORCID, Sophie Nambot ORCID, Antonio Vitobello ORCID, Ayesha Imtiaz ORCID and other authors.
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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