Journalartikel

Comprehensive Registration of DNA Sequence Variants Associated with Inherited Retinal Diseases in Leiden Open Variation Databases


AutorenlisteCremers, Frans P. M.; den Dunnen, Johan T.; Ajmal, Muhammad; Hussain, Alamdar; Preising, Markus N.; Daiger, Stephen P.; Qamar, Raheel

Jahr der Veröffentlichung2014

Seiten147-148

ZeitschriftHuman Mutation: Variation, Informatics and Disease

Bandnummer35

Heftnummer1

ISSN1059-7794

eISSN1098-1004

Open Access StatusGold

DOI Linkhttps://doi.org/10.1002/humu.22458

VerlagWiley



Zitierstile

Harvard-ZitierstilCremers, F., den Dunnen, J., Ajmal, M., Hussain, A., Preising, M., Daiger, S., et al. (2014) Comprehensive Registration of DNA Sequence Variants Associated with Inherited Retinal Diseases in Leiden Open Variation Databases, Human Mutation: Variation, Informatics and Disease, 35(1), pp. 147-148. https://doi.org/10.1002/humu.22458

APA-ZitierstilCremers, F., den Dunnen, J., Ajmal, M., Hussain, A., Preising, M., Daiger, S., & Qamar, R. (2014). Comprehensive Registration of DNA Sequence Variants Associated with Inherited Retinal Diseases in Leiden Open Variation Databases. Human Mutation: Variation, Informatics and Disease. 35(1), 147-148. https://doi.org/10.1002/humu.22458



Schlagwörter


ALLELESBBS1 MUTATIONSRETINITIS-PIGMENTOSA


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