Exome sequencing identifies a founder frameshift mutation in an alternative exon of USH1C as the cause of autosomal recessive retinitis pigmentosa with late-onset hearing loss (Q34516898)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Exome sequencing identifies a founder frameshift mutation in an alternative exon of USH1C as the cause of autosomal recessive retinitis pigmentosa with late-onset hearing loss |
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Exome sequencing identifies a founder frameshift mutation in an alternative exon of USH1C as the cause of autosomal recessive retinitis pigmentosa with late-onset hearing loss (English)
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Dror Sharon
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Samer Khateb
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Lina Zelinger
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Tamar Ben-Yosef
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Saul Merin
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Ornit Crystal-Shalit
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Menachem Gross
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Eyal Banin
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12 December 2012
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e51566
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12 December 2012
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