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Frosch M 1
Showing records 1 to 1 | Display all abstracts from Frosch M27990 Genome-wide homozygosity mapping and next generation sequencing indentifies SAMHD1 mutations in a novel variant of Aicardi-Goutieres syndrome
Du Moulin M; Thiele H; Barczyk K; George C; Frosch M; Schwindt W; Roth J; Nürnberg P; Rutsch F
European Journal of Pediatrics 2010; 169: 380-381
