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pro vyhledávání: '"Maigi Kulm"'
Autor:
Anshuman Verma, Vijayalakshmi Perumalsamy, Shashikant Shetty, Maigi Kulm, Periasamy Sundaresan
Publikováno v:
PLoS ONE, Vol 8, Iss 9, p e73172 (2013)
BACKGROUND: Leber congenital amaurosis (LCA) is the most severe form of inherited retinal visual impairment in children. So far, mutations in more than 20 genes have been known to cause LCA and among them, RPE65 is a suitable candidate for gene thera
Externí odkaz:
https://doaj.org/article/6442777083314d8c9bdfea86f44dcad0