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| 1 | Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy显示文摘 | Delmaghani S del Castillo FJ Michel V | 2006 | Nat Genet2006，38，： | 1 |
| 2 | Mutations in the gene encoding pejvakin,a newly identified protein of the afferent auditory pathway,cause DFNB59 auditory neuropathy显示文摘 | Delmaghani S del Castillo FJ Michel V | 2006 | Nat Genet2006，38，7： | 1 |
| 3 | Mutations in the gene encoding pejvakin,a newly identified protein of the afferent auditory pathway,cause DFNB59 auditory neuropathy 显示文摘 | Delmaghani S del Castillo FJ Michel V | 2006 | Nat Genet2006，38，7： | 1 |
| 4 | Mutations in the gene encoding pejvakin,a newly identified protein of the afferent auditory pathway,cause DFNB59 auditory neuropathy显示文摘 | Delmaghani S del Castillo FJ Michel V et el | 2006 | Nat Genet2006，38，： | 1 |
| 5 | Mutations in the gene encoding pejvakin,a newly identified protein of the afferent auditory pathway,cause DFNB59 auditory neuropathy显示文摘 | Delmaghani S Castillo FJ Michel V | 2006 | Nat Genet2006，38，7： | 1 |
| 6 | Mutations in the gene encoding pej-vakin,a newly identified protein of the afferent auditory pathway,cause DFNB59 auditory neuropathy显示文摘 | Delmaghani S del Castillo FJ Michel V Leibovici M Aghaie A Ron U Van Laer L Ben-Tal N Van Camp G Weil D Langa F Lathrop M Avan P Petit C | | 0，，07： | 1 |
| 7 | Mutations in the gene encoding pej-vakin,a newly identified protein of the afferent auditory pathway,cause DFNB59 auditory neuropathy显示文摘 | Delmaghani S del Castillo FJ Michel V Leibovici M Aghaie A Ron U Van Laer L Ben-Tal N Van Camp G Weil D Langa F Lathrop M Avan P Petit C | | 0，，07： | 1 |
| 8 | Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy 显示文摘 | DELMAGHANI S DEL CASTILLO F J MICHEL V | 2006 | Nat Genet2006，38，： | 1 |
| 9 | Mutations in the gene encoding pejvakin, a newly identified protein of the affer ent auditory pathway, cause DFNB59 auditory neuropathy显示文摘 | Delmaghani S del Castillo FJ Michel V | 2006 | Nat Genet2006，38，： | 1 |
| 10 | Mutations in the gene encoding pejvakin,anewly identified protein of the afferent auditory path-way,cause DFNB59auditory neuropathy显示文摘 | DELMAGHANI S DELCASTILLO F J MICHELV | 2006 | NatGenet2006，38，： | 1 |
| 11 | Mutations in the gene encoding pejvakin,a newly identified protein of the afferent auditory pathway,cause DFNB59 auditory neuropathy显示文摘 | DELMAGHANI S DEL CASTILLO F J MICHEL V | 2006 | Nat Genet2006，38，： | 1 |
| 12 | Defect in the gene encoding the EAR/EPTP domain- containing protein TSPEAR causes DFNB98 profound deafness显示文摘 | Delmaghani S Aghaie A Michalski N | 2012 | Hum MolGenet2012，21，： | 1 |
| 13 | 遗传性听神经病:从基因到病理机制显示文摘在过去的十年中,遗传学家们借助一批新技术推动了人们对遗传性耳聋更深入的认识。这些新技术的应用引发了一系列隐性、显性、X-连锁、Y-连锁和线粒体遗传相关性耳聋基因的发现。这一时期最重要的发现包括:常见隐性遗传性耳聋基因(如DFNB1,缝隙连接蛋白基因)、听神经病相关基因(DFNB9,otoferlin和DFNB59,pejvakin等)以及这些基因发生作用的分子机制等。 | Saaid Safieddine Sedigheh Delmaghani Isabelle Roux Christine Petit 袁慧军 | 2012 | 听力学及言语疾病杂志2012，20，1： | 0 |
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