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    Open Access

    TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations

    Precise genetic and phenotypic characterization of congenital stationary night blindness (CSNB) patients is needed for future therapeutic interventions. The aim of this study was to estimate the prevalence of ...

    Alaa AlTalbishi, Lina Zelinger, Christina Zeitz, Karen Hendler… in Scientific Reports (2019)

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