Autosomal recessive retinitis pigmentosa with homozygous rhodopsin mutation E150K and non-coding cis-regulatory variants in CRX-binding regions of SAMD7
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T. Langmann | M. Karlstetter | B. Leroy | M. Azam | R. Qamar | F. Depasse | Katharina Dannhausen | K. Van Schil | A. Aslanidis | E. de Baere