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Piryaei, Fahimeh and Pakmanesh, Rezvan and Salehirad, Maryam and Akbari, Soheila and Edizadeh, Masoud and Khodadadi, Hamidreza (2023) ALDH1A3-related congenital microphthalmia-8 due to a novel frameshift variant. European Journal of Medical Genetics.
Edizadeh, Masoud and Farajzadeh Valilou, Saeed and Karimzad Hagh, Javad and Salimi Asl, Mohammad and Abdi Rad, Isa (2021) A novel biallelic LMNB2 variant in a patient with progressive myoclonus epilepsy and ataxia: A case of laminopathy. Clin Case Rep.