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2. A novel mutation in the ALS2 gene in an iranian kurdish family with juvenile amyotrophic lateral sclerosis. Issue 1 (2nd January 2023)

5. COL18A1 is a candidate eye iridocorneal angle-closure gene in humans. (11th July 2018)

6. Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy. (4th May 2019)