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| The neuronal ceroid lipofuscinoses (Batten disease) S Mole, R Williams, H Goebel Oxford University Press, 2011 | 405* | 2011 |
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| The gene mutated in variant late-infantile neuronal ceroid lipofuscinosis (CLN6) and in nclf mutant mice encodes a novel predicted transmembrane protein RB Wheeler, JD Sharp, RA Schultz, JM Joslin, RE Williams, SE Mole The American Journal of Human Genetics 70 (2), 537-542, 2002 | 223 | 2002 |
| Kufs disease, the major adult form of neuronal ceroid lipofuscinosis, caused by mutations in CLN6 T Arsov, KR Smith, J Damiano, S Franceschetti, L Canafoglia, ... The American Journal of Human Genetics 88 (5), 566-573, 2011 | 190 | 2011 |
| Clinical challenges and future therapeutic approaches for neuronal ceroid lipofuscinosis SE Mole, G Anderson, HA Band, SF Berkovic, JD Cooper, SMK Holthaus, ... The Lancet Neurology 18 (1), 107-116, 2019 | 172 | 2019 |
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| CLN6, which is associated with a lysosomal storage disease, is an endoplasmic reticulum protein SE Mole, G Michaux, S Codlin, RB Wheeler, JD Sharp, DF Cutler Experimental cell research 298 (2), 399-406, 2004 | 142 | 2004 |
Hannah MitchisonUniversity College LondonVerified email at ucl.ac.uk
