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No Hot Spot Mutations CHRNE c.1327 delG, CHAT c.914T>C, and RAPSN c.264C>A in Iranian Patients with Congenital Myasthenic Syndrome.
Iran J Child Neurol. 2019 Spring;13(2):135-143.
Iran J Child Neurol. 2019.
PMID: 31037086
Free PMC article.
A Novel c.973G>T Mutation in the ε-subunit of the Acetylcholine Receptor Causing Congenital Myasthenic Syndrome in an Iranian Family.
Karimzadeh P, Parvizi Omran S, Ghaedi H, Omrani MD.
Karimzadeh P, et al. Among authors: parvizi omran s.
Balkan J Med Genet. 2019 Aug 28;22(1):95-98. doi: 10.2478/bjmg-2019-0010. eCollection 2019 Jun.
Balkan J Med Genet. 2019.
PMID: 31523627
Free PMC article.
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Association of Obesity-Related Genetic Variants (FTO and MC4R) with Breast Cancer Risk: A Population-Based Case-Control Study in Iran.
Mozafarizadeh M, Parvizi Omran S, Kordestani Z, Manshadi Dehghan H, Faridazar A, Houshmand M.
Mozafarizadeh M, et al. Among authors: parvizi omran s.
Iran J Biotechnol. 2019 Dec 1;17(4):e2460. doi: 10.30498/IJB.2019.99594. eCollection 2019 Dec.
Iran J Biotechnol. 2019.
PMID: 32671127
Free PMC article.
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