Table of contents

New loci

• Original article: Mutations in apoptosis-inducing factor cause X-linked recessive auditory neuropathy spectrum disorder (18 May, 2015)

  Liang Zong, Jing Guan, Megan Ealy, Qiujing Zhang, Dayong Wang, Hongyang Wang, Yali Zhao, Zhirong Shen, Colleen A Campbell, Fengchao Wang, Ju Yang, Wei Sun, Lan Lan, Dalian Ding, Linyi Xie, Yue Qi, Xin Lou, Xusheng Huang, Qiang Shi, Suhua Chang, Wenping Xiong, Zifang Yin, Ning Yu, Hui Zhao, Jun Wang, Jing Wang, Richard J Salvi, Christine Petit, Richard J H Smith, Qiuju Wang
• Original article:

  Mutations in the mitochondrial cysteinyl-tRNA synthase gene, CARS2, lead to a severe epileptic encephalopathy and complex movement disorder

  (18 March, 2015)

  Curtis R Coughlin, Gunter H Scharer, Marisa W Friederich, Hung-Chun Yu, Elizabeth A Geiger, Geralyn Creadon-Swindell, Abigail E Collins, Arnaud V Vanlander, Rudy Van Coster, Christopher A Powell, Michael A Swanson, Michal Minczuk, Johan L K Van Hove, Tamim H Shaikh
• Original article:

  Mutations in SLC1A4, encoding the brain serine transporter, are associated with developmental delay, microcephaly and hypomyelination

  (3 June, 2015)

  Nadirah Damseh, Alexandre Simonin, Chaim Jalas, Joseph A Picoraro, Avraham Shaag, Megan T Cho, Barak Yaacov, Julie Neidich, Motee Al-Ashhab, Jane Juusola, Sherri Bale, Aida Telegrafi, Kyle Retterer, John G Pappas, Ellen Moran, Joshua Cappell, Kwame Anyane Yeboa, Bassam Abu-Libdeh, Matthias A Hediger, Wendy K Chung, Orly Elpeleg, Simon Edvardson
• Short report:

  A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss

  (4 May, 2015)

  Ghulam Mujtaba, Julie M Schultz, Ayesha Imtiaz, Robert J Morell, Thomas B Friedman, Sadaf Naz