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Results: 1-2 |
Results: 2
Ocular phenotype of Bothnia dystrophy, an autosomal recessive retinitis pigmentosa associated with an R234W mutation in the RLBP1 gene
Authors: Burstedt, MSL Forsman-Semb, K Golovleva, I Janunger, T Wachtmeister, L Sandgren, O
Citation: Msl. Burstedt et al., Ocular phenotype of Bothnia dystrophy, an autosomal recessive retinitis pigmentosa associated with an R234W mutation in the RLBP1 gene, ARCH OPHTH, 119(2), 2001, pp. 260-267
Heart failure caused by a novel amyloidogenic mutation of the transthyretin gene: ATTR Ala45Ser
Authors: Janunger, T Anan, I Holmgren, G Lovheim, O Ohlsson, PI Suhr, OB Tashima, K
Citation: T. Janunger et al., Heart failure caused by a novel amyloidogenic mutation of the transthyretin gene: ATTR Ala45Ser, AMYLOID, 7(2), 2000, pp. 137-140
Risultati: 1-2 |