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Publicatie

Long-read sequencing to unravel complex structural variants of CEP78 leading to cone-rod dystrophy and hearing loss

Tijdschriftbijdrage - Tijdschriftartikel

Tijdschrift: FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY

ISSN: 2296-634X

Volume: 9

Jaar van publicatie:2021

WoS Id: 000647000400001
DOI: https://doi.org/10.3389/fcell.2021.664317
Handle: http://hdl.handle.net/1854/LU-8705421

Toegankelijkheid:Open

Zie ook: Long-read sequencing to unravel complex structural variants of CEP78 leading to cone-rod dystrophy and hearing loss
Zie ook: Long-Read Sequencing to Unravel Complex Structural Variants of CEP78 Leading to Cone-Rod Dystrophy and Hearing Loss.
Zie ook: Long-Read Sequencing to Unravel Complex Structural Variants of CEP78 Leading to Cone-Rod Dystrophy and Hearing Loss