Whole-Exome Sequencing Identifies Three Candidate Homozygous Variants in a Consanguineous Iranian Family with Autism Spectrum Disorder and Skeletal Problems
全外显子组测序在一个患有自闭症谱系障碍和骨骼问题的伊朗近亲结婚家庭中发现了三个候选纯合变异
期刊:Molecular Syndromology
影响因子:0.9
doi:10.1159/000506530
Farajzadeh Valilou, Saeed; Alavi, Afagh; Pashaei, Mahdiyeh; Ghasemi Firouzabadi, Saghar; Shafeghati, Yousef; Nozari, Ahoura; Hadipour, Fatemeh; Hadipour, Zahra; Maghsoodlou Estrabadi, Bijan; Gholamreza Noorazar, Seyed; Banihashemi, Susan; Karimian, Javad; Fattahi, Mahshid; Behjati, Farkhondeh