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Missense mutation in CEP78 in a family with cone-rod dystrophy, sensorineural hearing loss, obesity and subfertility

Giulia Ascari (UGent) , Stijn Van De Sompele (UGent) , Lara Derycke (UGent) , Gabriële Holtappels (UGent) , Olga Krysko (UGent) , Jo Van Dorpe (UGent) , David Creytens (UGent) , Thalia Van Laethem (UGent) , Irina Balikova (UGent) , Jan Gerris (UGent) , et al.
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MLA
Ascari, Giulia et al. “Missense Mutation in CEP78 in a Family with Cone-rod Dystrophy, Sensorineural Hearing Loss, Obesity and Subfertility.” Young Researcher Vision Camp, Abstracts. 2017. Print.
APA
Ascari, G., Van De Sompele, S., Derycke, L., Holtappels, G., Krysko, O., Van Dorpe, J., Creytens, D., et al. (2017). Missense mutation in CEP78 in a family with cone-rod dystrophy, sensorineural hearing loss, obesity and subfertility. Young Researcher Vision Camp, Abstracts. Presented at the Young Researcher Vision Camp (YRVC) 2017.
Chicago author-date
Ascari, Giulia, Stijn Van De Sompele, Lara Derycke, Gabriële Holtappels, Olga Krysko, Jo Van Dorpe, David Creytens, et al. 2017. “Missense Mutation in CEP78 in a Family with Cone-rod Dystrophy, Sensorineural Hearing Loss, Obesity and Subfertility.” In Young Researcher Vision Camp, Abstracts.
Chicago author-date (all authors)
Ascari, Giulia, Stijn Van De Sompele, Lara Derycke, Gabriële Holtappels, Olga Krysko, Jo Van Dorpe, David Creytens, Thalia Van Laethem, Irina Balikova, Jan Gerris, Claus Bachert, Bart Leroy, Elfride De Baere, and Frauke Coppieters. 2017. “Missense Mutation in CEP78 in a Family with Cone-rod Dystrophy, Sensorineural Hearing Loss, Obesity and Subfertility.” In Young Researcher Vision Camp, Abstracts.
Vancouver
1.
Ascari G, Van De Sompele S, Derycke L, Holtappels G, Krysko O, Van Dorpe J, et al. Missense mutation in CEP78 in a family with cone-rod dystrophy, sensorineural hearing loss, obesity and subfertility. Young Researcher Vision Camp, Abstracts. 2017.
IEEE
[1]
G. Ascari et al., “Missense mutation in CEP78 in a family with cone-rod dystrophy, sensorineural hearing loss, obesity and subfertility,” in Young Researcher Vision Camp, Abstracts, Leibertingen, Germany, 2017.
@inproceedings{8589094,
  author       = {Ascari, Giulia and Van De Sompele, Stijn and Derycke, Lara and Holtappels, Gabriële and Krysko, Olga and Van Dorpe, Jo and Creytens, David and Van Laethem, Thalia and Balikova, Irina and Gerris, Jan and Bachert, Claus and Leroy, Bart and De Baere, Elfride and Coppieters, Frauke},
  booktitle    = {Young Researcher Vision Camp, Abstracts},
  language     = {eng},
  location     = {Leibertingen, Germany},
  title        = {Missense mutation in CEP78 in a family with cone-rod dystrophy, sensorineural hearing loss, obesity and subfertility},
  year         = {2017},
}