Reply to: Pitfalls in the genetic testing of the OPN1LW-OPN1MW gene cluster in human subjects.

Haer-Wigman, Lonneke; den Ouden, Amber; Derks, Ronny; van Genderen, Maria M; Lugtenberg, Dorien; Verheij, Joke; Vijzelaar, Raymon; Yntema, Helger G; Vissers, Lisenka E L M; Neveling, Kornelia

Haer-Wigman, Lonneke; den Ouden, Amber; Derks, Ronny; van Genderen, Maria M; Lugtenberg, Dorien; Verheij, Joke; Vijzelaar, Raymon; Yntema, Helger G; Vissers, Lisenka E L M; Neveling, Kornelia.

Afiliación

Haer-Wigman L; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands. lonneke.haer-wigman@radboudumc.nl.
den Ouden A; Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, The Netherlands. lonneke.haer-wigman@radboudumc.nl.
Derks R; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
van Genderen MM; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Lugtenberg D; Bartiméus Diagnostic Center for complex visual disorders, Zeist, the Netherlands.
Verheij J; Department of Ophthalmology, University Medical Centre Utrecht, Utrecht, the Netherlands.
Vijzelaar R; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Yntema HG; Research Institute for Medical Innovation, Radboud University Medical Center, Nijmegen, The Netherlands.
Vissers LELM; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Neveling K; MRC Holland b v, Amsterdam, the Netherlands.

NPJ Genom Med ; 9(1): 29, 2024 May 04.

Article en En | MEDLINE | ID: mdl-38704388

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: NPJ Genom Med Año: 2024 Tipo del documento: Article País de afiliación: Países Bajos

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