Cone Dystrophy in Patient with Homozygous RP1L1 Mutation.
| Autor: | Kikuchi, Sachiko1 s9033@nms.ac.jp, Kameya, Shuhei1 shuheik@nms.ac.jp, Gocho, Kiyoko1 kknaka17@gmail.com, El Shamieh, Said2,3,4 said.shamieh@gmail.com, Akeo, Keiichiro1 akeo1226@nms.ac.jp, Sugawara, Yuko5 yuko-s@hyper.ocn.ne.jp, Yamaki, Kunihiko1 kyamaki@nms.ac.jp, Zeitz, Christina2,3,4 christina.zeitz@inserm.fr, Audo, Isabelle2,3,4,6 isabelle.audo@inserm.fr, Takahashi, Hiroshi7 tash@nms.ac.jp |
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| Zdroj: | BioMed Research International. 1/29/2015, Vol. 2015, p1-13. 13p. |
| Databáze: | Academic Search Ultimate |
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