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Analysis of mutations at the neurofibromatosis 1 (NF1) locus.
Hum Mol Genet. 1992 Dec;1(9):735-40. doi: 10.1093/hmg/1.9.735.
Hum Mol Genet. 1992.
PMID: 1302608
A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsies.
Nicholson GA, Valentijn LJ, Cherryson AK, Kennerson ML, Bragg TL, DeKroon RM, Ross DA, Pollard JD, McLeod JG, Bolhuis PA, et al.
Nicholson GA, et al. Among authors: cherryson ak.
Nat Genet. 1994 Mar;6(3):263-6. doi: 10.1038/ng0394-263.
Nat Genet. 1994.
PMID: 8012388
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The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3.
Nicholson GA, Dawkins JL, Blair IP, Kennerson ML, Gordon MJ, Cherryson AK, Nash J, Bananis T.
Nicholson GA, et al. Among authors: cherryson ak.
Nat Genet. 1996 May;13(1):101-4. doi: 10.1038/ng0596-101.
Nat Genet. 1996.
PMID: 8673084
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Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosis.
Hosler BA, Nicholson GA, Sapp PC, Chin W, Orrell RW, de Belleroche JS, Esteban J, Hayward LJ, Mckenna-Yasek D, Yeung L, Cherryson AK, Dench JE, Wilton SD, Laing NG, Horvitz HR, Brown RH Jr.
Hosler BA, et al. Among authors: cherryson ak.
Neuromuscul Disord. 1996 Oct;6(5):361-6. doi: 10.1016/0960-8966(96)00353-7.
Neuromuscul Disord. 1996.
PMID: 8938700
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