Recurrent KIF2A mutations are responsible for classic lissencephaly Mara CavallinEmilia K. BijlsmaNadia Bahi-Buisson Original Article 17 October 2016 Pages: 73 - 79
Analysis of gene expression in the nervous system identifies key genes and novel candidates for health and disease Sarah M CarpaniniThomas M WishartKim M Summers Original Article Open access 11 February 2017 Pages: 81 - 95
Identification and functional characterization of a novel MTFMT mutation associated with selective vulnerability of the visual pathway and a mild neurological phenotype Roberta La PianaWoranontee WeraarpachaiEric A. Shoubridge Short Communication 05 January 2017 Pages: 97 - 103
TFG associated hereditary spastic paraplegia: an addition to the phenotypic spectrum Huma TariqSadaf Naz Short Communication 25 January 2017 Pages: 105 - 109
ADCY5-related dyskinesia presenting as familial myoclonus-dystonia Andrew G. L. DouglasGaia AndreolettiNicola C. Foulds Short Communication Open access 22 February 2017 Pages: 111 - 117
Erratum to: PARP10 deficiency manifests by severe developmental delay and DNA repair defect Maher Awni ShahrourClaudia M. NicolaeOrly Elpeleg Erratum 11 February 2017 Pages: 119 - 119