Arch Iran Med. 2020;23(7): 426-433. doi: 10.34172/aim.2020.39

Original Article

Molecular Diagnosis of Hereditary Neuropathies by Whole Exome Sequencing and Expanding the Phenotype Spectrum

Sara Taghizadeh 1,2 ORCID, Raheleh Vazehan 3, Maryam Beheshtian 1,3 ORCID, Farnaz Sadeghinia 1, Zohreh Fattahi 1,3, Marzieh Mohseni 1,3, Sanaz Arzhangi 1, Shahriar Nafissi 4, Ariana Kariminejad 3, Hossein Najmabadi 1,3 * ORCID, Kimia Kahrizi 1 * ORCID

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Since we have many accepted case reports, we are not able to evaluate new ones until the first of January 2021.

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