Mutations in SPTLC1 , encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I
Nicholson, Garth A, Dawkins, Jennifer L, Hulme, Dennis J, Brahmbhatt, Sonal B, Auer-Grumbach, Michaela
Published in Nature genetics (01.03.2001)
Published in Nature genetics (01.03.2001)
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Exclusion of NFIL3 as the gene causing hereditary sensory neuropathy type I by mutation analysis
Hulme, Dennis J., Blair, Ian P., Dawkins, Jennifer L., Nicholson, Garth A.
Published in Human genetics (21.06.2000)
Published in Human genetics (21.06.2000)
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An enhanced linkage map of the sheep genome comprising more than 1000 loci
Maddox, J F, Davies, K P, Crawford, A M, Hulme, D J, Vaiman, D, Cribiu, E P, Freking, B A, Beh, K J, Cockett, N E, Kang, N, Riffkin, C D, Drinkwater, R, Moore, S S, Dodds, K G, Lumsden, J M, van Stijn, T C, Phua, S H, Adelson, D L, Burkin, H R, Broom, J E, Buitkamp, J, Cambridge, L, Cushwa, W T, Gerard, E, Galloway, S M, Harrison, B, Hawken, R J, Hiendleder, S, Henry, H M, Medrano, J F, Paterson, K A, Schibler, L, Stone, R T, van Hest, B
Published in Genome research (01.07.2001)
Published in Genome research (01.07.2001)
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