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Publicatie

Functional characterization of the first missense variant in CEP78, a founder allele associated with coneU+2010rod dystrophy, hearing loss and reduced male fertility

Tijdschriftbijdrage - Tijdschriftartikel

Tijdschrift: HUMAN MUTATION

ISSN: 1098-1004

Issue: 5

Volume: 41

Pagina's: 998 - 1011

Jaar van publicatie:2020

DOI: https://doi.org/10.1002/humu.23993
Handle: http://hdl.handle.net/1854/LU-8645355
WoS Id: 000512720600001

Toegankelijkheid:Open

Zie ook: Functional characterization of the first missense variant in CEP78, a founder allele associated with cone-rod dystrophy, hearing loss, and reduced male fertility
Zie ook: Functional characterization of the first missense variant in CEP78, a founder allele associated with cone-rod dystrophy, hearing loss, and reduced male fertility.