Showing 1 - 2 results of 2 for search 'Mangold, E', query time: 0.02s Refine Results
  1. 1
    The retinal phenotype associated with the frequent, synonymous c.783G > A mutation in CDHR1

    The retinal phenotype associated with the frequent, synonymous c.783G > A mutation in CDHR1 by Yusuf, IH, Gliem, M, Birtel, J, Muller, PL, Mangold, E, Bolz, H, Issa, PC

    Published 2018
    Conference item
  2. 2
    A specific macula-predominant retinal phenotype is associated with the CDHR1 variant c.783G>A, a silent mutation leading to in-frame exon skipping

    A specific macula-predominant retinal phenotype is associated with the CDHR1 variant c.783G>A, a silent mutation leading to in-frame exon skipping by Charbel Issa, P, Gliem, M, Yusuf, IH, Birtel, J, Müller, PL, Mangold, E, Downes, SM, MacLaren, RE, Betz, C, Bolz, HJ

    Published 2019
    Journal article

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