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                  <mods:namePart>Rodriguez-Martin, Carlos</mods:namePart>
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                  <mods:namePart>Cidre, Florencia</mods:namePart>
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                  <mods:namePart>Fernández-Teijeiro, Ana</mods:namePart>
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                  <mods:namePart>Gomez-Mariano, Gema Maria</mods:namePart>
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                  <mods:namePart>de la Vega, Leticia</mods:namePart>
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                  <mods:namePart>Ramos, Patricia</mods:namePart>
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                  <mods:namePart>Zaballos, Ángel</mods:namePart>
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                  <mods:namePart>Monzon-Fernandez, Sara</mods:namePart>
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                  <mods:namePart>Alonso, Javier</mods:namePart>
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                  <mods:namePart>Asociación Pablo Ugarte contra el cáncer infantil</mods:namePart>
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                     <mods:roleTerm type="text">funder</mods:roleTerm>
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                  <mods:namePart>Centro de Investigación Biomédica en Red - CIBERER (Enfermedades Raras)</mods:namePart>
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               <mods:name>
                  <mods:role>
                     <mods:roleTerm type="text">funder</mods:roleTerm>
                  </mods:role>
                  <mods:namePart>Red Temática de Investigación Cooperativa en Cáncer (RTICC) (España)</mods:namePart>
               </mods:name>
               <mods:name>
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                     <mods:roleTerm type="text">funder</mods:roleTerm>
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                  <mods:namePart>Miguelañez</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2024-01-23T13:39:16Z</mods:dateAccessioned>
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                  <mods:dateAvailable encoding="iso8601">2024-01-23T13:39:16Z</mods:dateAvailable>
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               <mods:originInfo>
                  <mods:dateIssued encoding="iso8601">2016-05</mods:dateIssued>
               </mods:originInfo>
               <mods:identifier type="citation">J Hum Genet. 2016 May;61(5):463-6.</mods:identifier>
               <mods:identifier type="doi">10.1038/jhg.2015.173</mods:identifier>
               <mods:identifier type="e-issn">1435-232X</mods:identifier>
               <mods:identifier type="journal">Journal of human genetics</mods:identifier>
               <mods:identifier type="pubmedID">26763876</mods:identifier>
               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/17263</mods:identifier>
               <mods:abstract>Retinoblastoma (RB, MIM 180200) is the paradigm of hereditary cancer. Individuals harboring a constitutional mutation in one allele of the RB1 gene have a high predisposition to develop RB. Here, we present the first case of familial RB caused by a de novo insertion of a full-length long interspersed element-1 (LINE-1) into intron 14 of the RB1 gene that caused a highly heterogeneous splicing pattern of RB1 mRNA. LINE-1 insertion was inferred by mRNA studies and full-length sequenced by massive parallel sequencing. Some of the aberrant mRNAs were produced by noncanonical acceptor splice sites, a new finding that up to date has not been described to occur upon LINE-1 retrotransposition. Our results clearly show that RNA-based strategies have the potential to detect disease-causing transposon insertions. It also confirms that the incorporation of new genetic approaches, such as massive parallel sequencing, contributes to characterize at the sequence level these unique and exceptional genetic alterations.</mods:abstract>
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                  <mods:title>Familial retinoblastoma due to intronic LINE-1 insertion causes aberrant and noncanonical mRNA splicing of the RB1 gene</mods:title>
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               <mods:genre>research article</mods:genre>
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