Items where Author is "Kim, D. S."
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(2015) Homozygous MAPT R406W mutation causing FTDP phenotype: A unique instance of a unique mutation. Gene. pp. 150-152. ISSN 0378-1119
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(2015) Homozygous MAPT R406W mutation causing FTDP phenotype: A unique instance of a unique mutation. Gene. pp. 150-152. ISSN 0378-1119