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Novel truncating mutation in CACNA1F in a young male patient diagnosed with optic atrophy.

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Title: Novel truncating mutation in CACNA1F in a young male patient diagnosed with optic atrophy.
Authors: Pasutto, Francesca1 francesca.pasutto@uk-erlangen.de, Ekici, Arif1, Reis, André1, Kremers, Jan2, Huchzermeyer, Cord2
Source: Ophthalmic Genetics. Dec2018, Vol. 39 Issue 6, p741-748. 8p.
Database: Academic Search Ultimate
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PubType: Academic Journal
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  Data: Novel truncating mutation in CACNA1F in a young male patient diagnosed with optic atrophy.
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  Data: <searchLink fieldCode="AR" term="%22Pasutto%2C+Francesca%22">Pasutto, Francesca</searchLink><relatesTo>1</relatesTo><i> francesca.pasutto@uk-erlangen.de</i><br /><searchLink fieldCode="AR" term="%22Ekici%2C+Arif%22">Ekici, Arif</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Reis%2C+André%22">Reis, André</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Kremers%2C+Jan%22">Kremers, Jan</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Huchzermeyer%2C+Cord%22">Huchzermeyer, Cord</searchLink><relatesTo>2</relatesTo>
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  Data: <searchLink fieldCode="JN" term="%22Ophthalmic+Genetics%22">Ophthalmic Genetics</searchLink>. Dec2018, Vol. 39 Issue 6, p741-748. 8p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=133290715
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      – Type: doi
        Value: 10.1080/13816810.2018.1520263
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      – Code: eng
        Text: English
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      – TitleFull: Novel truncating mutation in CACNA1F in a young male patient diagnosed with optic atrophy.
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            NameFull: Pasutto, Francesca
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            NameFull: Ekici, Arif
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            NameFull: Reis, André
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              M: 12
              Text: Dec2018
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              Y: 2018
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              Value: 39
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