B. A. Chioza
University of Exeter Medical School
43 papers found
Refreshing results…
SLITRK6 mutations cause myopia and deafness in humans and mice
Download from www.jci.orgDeficiency of terminal ADP-ribose protein glycohydrolase TARG1/C6orf130 in neurodegenerative disease
Download from www.ncbi.nlm.nih.govMutation of HERC2 causes developmental delay with Angelman-like features
Download from nbn-resolving.deDefective Presynaptic Choline Transport Underlies Hereditary Motor Neuropathy
Download from www.ncbi.nlm.nih.govLinkage of monogenic infantile hypertrophic pyloric stenosis to chromosome 16q24
Download from www.nature.comLinkage and mutational analysis of CLCN2 in childhood absence epilepsy
Download from www.researchgate.netLinkage and association analysis of CACNG3 in childhood absence epilepsy
Download from www.nature.comEvaluation of CACNA1H in European patients with childhood absence epilepsy
Download from www.researchgate.netMissing publications? Search for publications with a matching author name.