Journal article

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


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

Publication year2014

Pages147-148

JournalHuman Mutation: Variation, Informatics and Disease

Volume number35

Issue number1

ISSN1059-7794

eISSN1098-1004

Open access statusGold

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

PublisherWiley



Citation Styles

Harvard Citation styleCremers, 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 Citation styleCremers, 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



Keywords


ALLELESBBS1 MUTATIONSRETINITIS-PIGMENTOSA

Last updated on 2025-10-06 at 10:16