Your browser doesn't support javascript.
loading
Correction: Littink, K. W.; et al. Autosomal Recessive NRL Mutations in Patients with Enhanced S-Cone Syndrome. Genes 2018, 9, 68.
Littink, Karin W; Stappers, Patricia T Y; Riemslag, Frans C C; Talsma, Herman E; van Genderen, Maria M; Cremers, Frans P M; Collin, Rob W J; van den Born, L Ingeborgh.
Afiliação
  • Littink KW; The Rotterdam Eye Hospital, 3011 BH Rotterdam, The Netherlands. k.littink@oogziekenhuis.nl.
  • Stappers PTY; The Rotterdam Eye Hospital, 3011 BH Rotterdam, The Netherlands. p.stappers@oogziekenhuis.nl.
  • Riemslag FCC; The Rotterdam Eye Hospital, 3011 BH Rotterdam, The Netherlands. FRiemslag@gmail.com.
  • Talsma HE; Bartiméus Center for Complex Visual Disorders, 3703 AJ Zeist, The Netherlands. FRiemslag@gmail.com.
  • van Genderen MM; The Rotterdam Eye Hospital, 3011 BH Rotterdam, The Netherlands. HTalsma@bartimeus.nl.
  • Cremers FPM; Bartiméus Center for Complex Visual Disorders, 3703 AJ Zeist, The Netherlands. HTalsma@bartimeus.nl.
  • Collin RWJ; Bartiméus Center for Complex Visual Disorders, 3703 AJ Zeist, The Netherlands. mvgenderen@bartimeus.nl.
  • van den Born LI; Department of Human Genetics, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands. Frans.Cremers@radboudumc.nl.
Genes (Basel) ; 9(3)2018 03 07.
Article em En | MEDLINE | ID: mdl-29518905
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Genes (Basel) Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Holanda
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Genes (Basel) Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Holanda