Titre : | Molecular Diagnosis of Hereditary Neuropathies by Whole Exome Sequencing and Expanding the Phenotype Spectrum |
Revue : | Archives of iranian medicine, 23, 7 |
Auteurs : | Taghizadeh S ; Vazehan R ; Beheshtian M ; Sadeghinia F ; Fattahi Z ; Mohseni M ; Arzhangi S ; Nafissi S ; Kariminejad A ; Najmabadi H ; Kahrizi K |
Type de document : | Article |
Editeur : | Iran, 2020 |
Pages : | p 426 |
Langues: | Anglais |
Mots-clés: | Charcot-Marie-Tooth disease;inherited peripheral neuropathy;whole exome sequencing; |
Pubmed / DOI : | Pubmed : 32657593 / DOI : 10.34172/aim.2020.39 |
N° Profil MNM : | 2020071 |
En ligne : | http://www.ncbi.nlm.nih.gov/pubmed/32657593 |