Search Results - "Fallström, M"
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Mutation screening of patients with Alzheimer disease identifies APP locus duplication in a Swedish patient
Published in BMC research notes (01-11-2011)“…Missense mutations in three different genes encoding amyloid-β precursor protein, presenilin 1 and presenilin 2 are recognized to cause familial early-onset…”
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Journal Article -
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Spectrum of mutations in the CFTR gene of patients with classical and atypical forms of cystic fibrosis from southwestern Sweden: identification of 12 novel mutations
Published in Genetic testing (01-09-2001)“…Cystic fibrosis (CF) is caused by mutations in the CFTR gene. The spectrum of CFTR mutations varies between populations and depends on different factors, such…”
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Journal Article