Browsing by Keyword : *Point Mutation

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Showing results 1 to 2 of 2

Publication YearTitleAJOU
Author
2004A novel point mutation in PMP22 gene associated with a familial case of Charcot-Marie-Tooth disease type 1A with sensorineural deafness.주인수허균
1997Gain or loss of diabetogenicity resulting from a single point mutation in recombinant encephalomyocarditis virus.강엽윤지원
1

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