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  • Ascari, G (author)

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

  • Article/chapterEnglish2020

Publisher, publication year, extent ...

  • 2020-02-12
  • Hindawi Limited,2020

Numbers

  • LIBRIS-ID:oai:prod.swepub.kib.ki.se:142967805
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:142967805URI
  • https://doi.org/10.1002/humu.23993DOI

Supplementary language notes

  • Language:English

Part of subdatabase

Classification

  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Added entries (persons, corporate bodies, meetings, titles ...)

  • Peelman, F (author)
  • Farinelli, P (author)
  • Rosseel, T (author)
  • Lambrechts, N (author)
  • Wunderlich, KA (author)
  • Wagner, M (author)
  • Nikopoulos, K (author)
  • Martens, P (author)
  • Balikova, I (author)
  • Derycke, L (author)
  • Holtappels, G (author)
  • Krysko, O (author)
  • Van Laethem, T (author)
  • De Jaegere, S (author)
  • Guillemyn, B (author)
  • De Rycke, R (author)
  • De Bleecker, J (author)
  • Creytens, D (author)
  • Van Dorpe, J (author)
  • Gerris, J (author)
  • Bachert, CKarolinska Institutet (author)
  • Neuhofer, C (author)
  • Walraedt, S (author)
  • Bischoff, A (author)
  • Pedersen, LB (author)
  • Klopstock, T (author)
  • Rivolta, C (author)
  • Leroy, BP (author)
  • De Baere, E (author)
  • Coppieters, F (author)
  • Karolinska Institutet (creator_code:org_t)

Related titles

  • In:Human mutation: Hindawi Limited41:5, s. 998-10111098-10041059-7794

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