Zobrazeno 1 - 3
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pro vyhledávání: '"ciliogenesis repair"'
Autor:
Xavier Gerard, Isabelle Perrault, Sylvain Hanein, Eduardo Silva, Karine Bigot, Sabine Defoort-Delhemmes, Marlèene Rio, Arnold Munnich, Daniel Scherman, Josseline Kaplan, Antoine Kichler, Jean-Michel Rozet
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 1, Iss C (2012)
Leber congenital amaurosis (LCA) is a severe hereditary retinal dystrophy responsible for congenital or early-onset blindness. The most common disease-causing mutation (>10%) is located deep in intron 26 of the CEP290 gene (c.2991+1655A>G). It create
Externí odkaz:
https://doaj.org/article/4c6ac99f7bf04c2eb9a5d0e5fd83e9c1
Autor:
Sabine Defoort-Delhemmes, Xavier Gérard, Arnold Munnich, Eduardo Ferreira da Silva, Jean-Michel Rozet, Sylvain Hanein, Daniel Scherman, Marlèene Rio, Isabelle Perrault, Antoine Kichler, Karine Bigot, Josseline Kaplan
Publikováno v:
Molecular Therapy. Nucleic Acids
ResearcherID
Molecular Therapy: Nucleic Acids, Vol 1, Iss C (2012)
ResearcherID
Molecular Therapy: Nucleic Acids, Vol 1, Iss C (2012)
Leber congenital amaurosis (LCA) is a severe hereditary retinal dystrophy responsible for congenital or early-onset blindness. The most common disease-causing mutation (>10%) is located deep in intron 26 of the CEP290 gene (c.2991+1655A>G). It create
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26cc441104c9a7c34f926e3b30827ac4
https://pubmed.ncbi.nlm.nih.gov/23344081
https://pubmed.ncbi.nlm.nih.gov/23344081
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