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Science, ISSN 0036-8075, 5/2009, Volume 324, Issue 5930, pp. 1035 - 1044
Journal Article
BMC Genomics, ISSN 1471-2164, 01/2018, Volume 19, Issue 1, pp. 46 - 46
Journal Article
BMC Medical Genetics, ISSN 1471-2350, 05/2018, Volume 19, Issue 1, pp. 72 - 72
Background: Infantile neuroaxonal dystrophy (INAD) is a rare hereditary neurological disorder caused by mutations in PLA2G6. The disease commonly affects... 
Infantile neuroaxonal dystrophy | PLA2G6 | Whole exome sequencing | Sudan | NEURODEGENERATION | GENETICS & HEREDITY | Nervous system diseases | Usage | Genetic aspects | Research | Nucleotide sequencing | DNA sequencing | Index Medicus | Life Sciences | Genetics | Human genetics
Journal Article
Journal Article
by Jallow, Muminatou and Molyneux, Malcolm E and Singhasivanon, Pratap and Parker, Michael and Donnelly, Peter and Clark, Taane G and Mueller, Ivo and Pinder, Margaret and Karunaweera, Nadira and Dolo, Amagana and Fry, Andrew E and Gwilliam, Rhian and Bojang, Kalifa A and Williams, Thomas N and Amodu, Olukemi and Horstmann, Rolf D and Kokwaro, Gilbert and Rowlands, Kate and Drakeley, Chris and Auburn, Sarah and Bumpstead, Suzannah J and Doumbo, Ogobara K and Achidi, Eric Akum and Agbenyega, Tsiri and Peshu, Norbert and Somaskantharajah, Elilan and Mendy, Alieu and Dunstan, Sarah and Marchini, Jonathan and Lemnge, Martha and Teo, Yik Ying and Tall, Adama and Ibrahim, Muntaser and Deloukas, Panos and Makani, Julie and Rockett, Kirk A and Green, Angela and Jeffreys, Anna E and Sirima, Sodiomon and Koram, Kwadwo A and Campino, Susana and Morris, Andrew and Modiano, David and Corran, Patrick and Sisay-Joof, Fatou and Troye-Blomberg, Marita and Fernando, Deepika and Riley, Eleanor M and Potter, Simon and Evans, Jennifer and Sakuntabhai, Anavaj and Conway, David J and Widden, Claire and Ragoussis, Jiannis and Allen, Angela and Hien, Tran Tinh and Inouye, Michael and Palotie, Aarno and Sirugo, Giorgio and Taylor, Terrie E and Howie, Bryan and Kwiatkowski, Dominic P and Thera, Mahamadou and Kivinen, Katja and Small, Kerrin S and Puijalon, Odile and Hunt, Sarah E and Djimde, Abdoulaye and Farrar, Jeremy and Reyburn, Hugh and Marsh, Kevin and Michon, Pascal and Wilson, Michael and Usen, Stanley and Coffey, Alison and SanJoaquin, Miguel and Plowe, Christopher V and Reeder, John and Rogers, Jane and Dunham, Andrew and Whittaker, Pamela and Wellcome Trust Case Control Consor and Malaria Genomic Epidemiology Netwo and Wellcome Trust Case Control Consortium and Malaria Genomic Epidemiology Network and Naturvetenskapliga fakulteten and Stockholms universitet and Avdelningen för immunologi and Wenner-Grens institut
Nature Genetics, ISSN 1061-4036, 06/2009, Volume 41, Issue 6, pp. 657 - 665
Journal Article