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

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Bibliographic Details
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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