Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene (Q24531671)
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Current Data About Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene
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(P1476) "Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene" (language: en)

(P2093) A I den Hollander
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J R Heckenlively
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L I van den Born
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Y J de Kok
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S D van der Velde-Visser
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U Kellner
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B Jurklies
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M J van Schooneveld
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A Blankenagel
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K Rohrschneider
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B Wissinger
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J R Cruysberg
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A F Deutman
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H G Brunner
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E Apfelstedt-Sylla
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C B Hoyng
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F P Cremers
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(P854) https://pubmed.ncbi.nlm.nih.gov/11389483
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(P854) https://pubmed.ncbi.nlm.nih.gov/11389483
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External Links
(P356) 10.1086/321263
(P698) 11389483
(P932) 1226034
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