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

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Zeitschriftentitel: PLOS ONE
Personen und Körperschaften: Micheal, Shazia, Siddiqui, Sorath Noorani, Zafar, Saemah Nuzhat, Villanueva-Mendoza, Cristina, Cortés-González, Vianney, Khan, Muhammad Imran, den Hollander, Anneke I.
In: PLOS ONE, 11, 2016, 7, S. e0160016
Format: E-Article
Sprache: Englisch
veröffentlicht:
Public Library of Science (PLoS)
Schlagwörter:
Multidisciplinary
author_facet Micheal, Shazia
Siddiqui, Sorath Noorani
Zafar, Saemah Nuzhat
Villanueva-Mendoza, Cristina
Cortés-González, Vianney
Khan, Muhammad Imran
den Hollander, Anneke I.
Micheal, Shazia
Siddiqui, Sorath Noorani
Zafar, Saemah Nuzhat
Villanueva-Mendoza, Cristina
Cortés-González, Vianney
Khan, Muhammad Imran
den Hollander, Anneke I.
author Micheal, Shazia
Siddiqui, Sorath Noorani
Zafar, Saemah Nuzhat
Villanueva-Mendoza, Cristina
Cortés-González, Vianney
Khan, Muhammad Imran
den Hollander, Anneke I.
spellingShingle Micheal, Shazia
Siddiqui, Sorath Noorani
Zafar, Saemah Nuzhat
Villanueva-Mendoza, Cristina
Cortés-González, Vianney
Khan, Muhammad Imran
den Hollander, Anneke I.
PLOS ONE
A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
Multidisciplinary
author_sort micheal, shazia
spelling Micheal, Shazia Siddiqui, Sorath Noorani Zafar, Saemah Nuzhat Villanueva-Mendoza, Cristina Cortés-González, Vianney Khan, Muhammad Imran den Hollander, Anneke I. 1932-6203 Public Library of Science (PLoS) Multidisciplinary http://dx.doi.org/10.1371/journal.pone.0160016 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma PLOS ONE
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title A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
title_unstemmed A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
title_full A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
title_fullStr A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
title_full_unstemmed A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
title_short A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
title_sort a novel homozygous mutation in foxc1 causes axenfeld rieger syndrome with congenital glaucoma
topic Multidisciplinary
url http://dx.doi.org/10.1371/journal.pone.0160016
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author Micheal, Shazia, Siddiqui, Sorath Noorani, Zafar, Saemah Nuzhat, Villanueva-Mendoza, Cristina, Cortés-González, Vianney, Khan, Muhammad Imran, den Hollander, Anneke I.
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spelling Micheal, Shazia Siddiqui, Sorath Noorani Zafar, Saemah Nuzhat Villanueva-Mendoza, Cristina Cortés-González, Vianney Khan, Muhammad Imran den Hollander, Anneke I. 1932-6203 Public Library of Science (PLoS) Multidisciplinary http://dx.doi.org/10.1371/journal.pone.0160016 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma PLOS ONE
spellingShingle Micheal, Shazia, Siddiqui, Sorath Noorani, Zafar, Saemah Nuzhat, Villanueva-Mendoza, Cristina, Cortés-González, Vianney, Khan, Muhammad Imran, den Hollander, Anneke I., PLOS ONE, A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma, Multidisciplinary
title A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
title_full A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
title_fullStr A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
title_full_unstemmed A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
title_short A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
title_sort a novel homozygous mutation in foxc1 causes axenfeld rieger syndrome with congenital glaucoma
title_unstemmed A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
topic Multidisciplinary
url http://dx.doi.org/10.1371/journal.pone.0160016