Personalkatalog

Malin Olsson

Kontaktinformation
Befattning:	Forskningsingenjör, förste
Verksam vid:	Medicinsk biovetenskap
Avdelning:	Medicinsk och klinisk genetik
Adress:	Umeå universitet SE-901 85 Umeå Sverige
Besöksadress:	By 6M, vån 3, Sjukhusområdet, 5125
Tel:	+46 90 785 16 21

Författare	Titel	År	Fulltext
Norgren, Nina Hellman, Urban Ericzon, Bo Goran; et al.	Allele specific expression of the transthyretin gene in Swedish patients with hereditary transthyretin amyloidosis (ATTR V30M) is similar between the two alleles PLoS ONE, 7(11): e49981-	2012	Hämta
Bonaïti, Bernard Olsson, Malin Hellman, Urban; et al.	TTR familial amyloid polyneuropathy: does a mitochondrial polymorphism entirely explain the parent-of-origin difference in penetrance? European Journal of Human Genetics	2010	-
Olsson, Malin	Familial amyloidosis with polyneuropathy: studies of genetic factors modifying the phenotype of the disease	2010	Hämta
Olsson, Malin Norgren, Nina Obayashi, Konen; et al.	A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V30M carriers BMC Medical Genetics, 11: 130-	2010	-
Suhr, Ole B Andersen, Oluf Aronsson, Thomas; et al.	Report of five rare or previously unknown amyloidogenic transthyretin mutations disclosed in Sweden. Amyloid, 16(4): 208-214	2009	-
Olsson, Malin Hellman, Urban Planté-Bordeneuve, V; et al.	Mitochondrial haplogroup is associated with the phenotype of familial amyloidosis with polyneuropathy in Swedish and French patients Clinical Genetics, 75(2): 163-168	2009	-

Sidansvarig: Åsa Lundsten
2010-11-02