(Q37114821)
Statements
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Screening for duplications, deletions and a common intronic mutation detects 35% of second mutations in patients with USH2A monoallelic mutations on Sanger sequencing (English)
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Mireille Claustres
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Maria Bitner-Glindzicz
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Linda M Luxon
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Polona Le Quesne Stabej
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Heather B Steele-Stallard
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Eva Lenassi
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Anne-Francoise Roux
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Andrew R Webster
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8 August 2013
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Identifiers
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