A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma

• Shazia Micheal,

  Affiliation Department of Ophthalmology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands

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• Sorath Noorani Siddiqui ,

  Contributed equally to this work with: Sorath Noorani Siddiqui, Saemah Nuzhat Zafar

  Affiliation Department of Pediatric Ophthalmology, Al-Shifa Eye Trust Hospital, Jhelum Road, Rawalpindi, Pakistan

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• Saemah Nuzhat Zafar ,

  Contributed equally to this work with: Sorath Noorani Siddiqui, Saemah Nuzhat Zafar

  Affiliation Department of Pediatric Ophthalmology, Al-Shifa Eye Trust Hospital, Jhelum Road, Rawalpindi, Pakistan

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• Cristina Villanueva-Mendoza,

  Affiliation Genetics Department Asociación Para Evitar la Ceguera en México, Coyoacán, Mexico

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• Vianney Cortés-González,

  Affiliation Genetics Department Asociación Para Evitar la Ceguera en México, Coyoacán, Mexico

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• Muhammad Imran Khan,

  Affiliation Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands

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• Anneke I. den Hollander

  * E-mail: Anneke.denHollander@radboudumc.nl

  Affiliations Department of Ophthalmology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands, Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands

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