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Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factor.
Al-Chalabi A, Andersen PM, Chioza B, Shaw C, Sham PC, Robberecht W, Matthijs G, Camu W, Marklund SL, Forsgren L, Rouleau G, Laing NG, Hurse PV, Siddique T, Leigh PN, Powell JF. Al-Chalabi A, et al. Among authors: matthijs g. Hum Mol Genet. 1998 Dec;7(13):2045-50. doi: 10.1093/hmg/7.13.2045. Hum Mol Genet. 1998. PMID: 9817920
TDP-43 M311V mutation in familial amyotrophic lateral sclerosis.
Lemmens R, Race V, Hersmus N, Matthijs G, Van Den Bosch L, Van Damme P, Dubois B, Boonen S, Goris A, Robberecht W. Lemmens R, et al. Among authors: matthijs g. J Neurol Neurosurg Psychiatry. 2009 Mar;80(3):354-5. doi: 10.1136/jnnp.2008.157677. J Neurol Neurosurg Psychiatry. 2009. PMID: 19228676 No abstract available.
Primary autosomal recessive microcephaly: MCPH5 maps to 1q25-q32.
Jamieson CR, Fryns JP, Jacobs J, Matthijs G, Abramowicz MJ. Jamieson CR, et al. Among authors: matthijs g. Am J Hum Genet. 2000 Dec;67(6):1575-7. doi: 10.1086/316909. Epub 2000 Nov 6. Am J Hum Genet. 2000. PMID: 11067780 Free PMC article.
349 results