A Novel c.973G>T Mutation in the ε-subunit of the Acetylcholine Receptor Causing Congenital Myasthenic Syndrome in an Iranian Family

por Karimzadeh, P, Parvizi Omran, S, Ghaedi, H, Omrani, MD
Publicado 2019

No Hot Spot Mutations CHRNE c.1327 delG, CHAT c.914T>C, and RAPSN c.264C>A in Iranian Patients with Congenital Myasthenic Syndrome

por PARVIZI OMRAN, Sima, HOUSHMAND, Massod, DOMINIC, Donkor, FARJAMI, Zahra, KARIMZADEH, Parvaneh
Publicado 2019

Association of Obesity-Related Genetic Variants (FTO and MC4R) with Breast Cancer Risk: A Population-Based Case–Control Study in Iran

por Mozafarizadeh, Mina, Parvizi Omran, Sima, Kordestani, Zeinab, Manshadi Dehghan, Hamidreza, Faridazar, Alireza, Houshmand, Massoud
Publicado 2019