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Variability in clinical phenotypes of PRPF8 -linked autosomal dominant retinitis pigmentosa correlates with differential PRPF8/SNRNP200 interactions.

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Title: Variability in clinical phenotypes of PRPF8 -linked autosomal dominant retinitis pigmentosa correlates with differential PRPF8/SNRNP200 interactions.
Authors: Escher, Pascal1,2,3 (AUTHOR) veronika.vaclavik@fa2.ch, Passarin, Olga1 (AUTHOR), Munier, Francis L.1 (AUTHOR), Tran, Viet H.1 (AUTHOR), Vaclavik, Veronika1,4 (AUTHOR) veronika.vaclavik@fa2.ch
Source: Ophthalmic Genetics. Jan/Feb2018, Vol. 39 Issue 1, p80-86. 7p.
Database: Academic Search Ultimate
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  Data: Variability in clinical phenotypes of PRPF8 -linked autosomal dominant retinitis pigmentosa correlates with differential PRPF8/SNRNP200 interactions.
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  Data: <searchLink fieldCode="JN" term="%22Ophthalmic+Genetics%22">Ophthalmic Genetics</searchLink>. Jan/Feb2018, Vol. 39 Issue 1, p80-86. 7p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=126867193
RecordInfo BibRecord:
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      – Type: doi
        Value: 10.1080/13816810.2017.1393825
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      – Code: eng
        Text: English
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        PageCount: 7
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      – TitleFull: Variability in clinical phenotypes of PRPF8 -linked autosomal dominant retinitis pigmentosa correlates with differential PRPF8/SNRNP200 interactions.
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            NameFull: Escher, Pascal
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            NameFull: Passarin, Olga
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            NameFull: Munier, Francis L.
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            NameFull: Tran, Viet H.
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            NameFull: Vaclavik, Veronika
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            – D: 01
              M: 01
              Text: Jan/Feb2018
              Type: published
              Y: 2018
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              Value: 39
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            – TitleFull: Ophthalmic Genetics
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