Author Response: Penetrance of the ABCA4 p.Asn1868Ile Allele in Stargardt Disease.

Cremers, Frans P M; Cornelis, Stéphanie S; Runhart, Esmee H; Astuti, Galuh D N

Cremers, Frans P M; Cornelis, Stéphanie S; Runhart, Esmee H; Astuti, Galuh D N.

Afiliación

Cremers FPM; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Cornelis SS; Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
Runhart EH; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Astuti GDN; Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.

Invest Ophthalmol Vis Sci ; 59(13): 5566-5568, 2018 11 01.

Article en En | MEDLINE | ID: mdl-30480704

Asunto(s)

Degeneración Macular/genética; Transportadoras de Casetes de Unión a ATP/genética; Alelos; Análisis Mutacional de ADN; Humanos; Degeneración Macular/congénito; Penetrancia; Enfermedad de Stargardt

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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Degeneración Macular Límite: Humans Idioma: En Revista: Invest Ophthalmol Vis Sci Año: 2018 Tipo del documento: Article País de afiliación: Países Bajos

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