Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsi... by Zahra Nouri, Akram Sarmadi, Sina Narrei, Hamidreza Kianersi, Farzan Kianersi, Mohammad Amin Tabatabaiefar

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Correction: Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and... by Zahra Nouri, Akram Sarmadi, Sina Narrei, Hamidreza Kianersi, Farzan Kianersi, Mohammad Amin Tabatabaiefar

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A novel NBN germline mutation as the likely inherited etiology of various cancer types in an Iranian family by Akram Sarmadi, Samaneh Adelian, Zahra Nouri, Shaghayegh Haghjooy Javanmard, Rasoul Omidzadeh, Mohammad Amin Tabatabaiefar

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A novel missense pathogenic variant c.9455T > G (p.L3152R) in CDH23 underlies autosomal recessive non-syndromic hearing loss by Ladan Sadeghian, Marziyeh Hoseinzadeh, Mohammad reza Pourreza, Saeed Khalili, Najmeh Fattahi, Mohammad Amin Tabatabaiefar

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A Novel Homozygote Pathogenic Variant in the DIAPH1 Gene Associated With Seizures, Cortical Blindness, and Microcephaly Syndrome (SCBMS): Report of a Family and Literature Review by Emran Esmaeilzadeh, Sajjad Biglari, Meysam Mosallaei, Hamid Reza Khorram Khorshid, Hassan Vahidnezhad, Mohammad Amin Tabatabaiefar

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Correction: whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical fea... by Atefeh Mir, Yongjun Song, Hane Lee, Hossein Khanahmad, Erfan Khorram, Jafar Nasiri, Mohammad Amin Tabatabaiefar

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Sero-molecular prevalence of toxoplasmosis in hemodialysis and peritoneal dialysis patients in Markazi Province, Iran by Hossein Sarmadian, Mana Shojapour, Fereshteh chegeni, Mohammad Amin Tabatabaiefar, Farshid Haghverdi, Roham Sarmadian, Reza Ghasemikhah

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New Insight into Pathogenic Variant p.L275P on the Structure and Function of Steroidogenic Acute Regulatory Protein (STAR) Through Molecular Dynamics Simulation by Shahrzad Aghaei, Mohammad Amin Tabatabaiefar, Javad Saffari-Chaleshtori, Erfan Korram, Sara Sadeghi Amini, Maryam Aghaei, Mahbobeh Koohiyan, Zahra Ataie, Payam Samei, Effat Farrokhi

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Investigating TSHR gene variants in consanguineous families: novel insights into variable expression in familial congenital hypothyroidism by Zakiye Nadeali, Zakiye Nadeali, Zohreh Mohammadi-Zaniani, Sajjad Biglari, Newsha Molavi, Khashayar Zardoui, Sam Mirfendereski, Mahin Hashemipour, Mahin Hashemipour, Mohammad Amin Tabatabaiefar, Constantin Polychronakos

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