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Novel ADAR1 mutations including a single amino acid deletion in the deaminase domain underlie dyschromatosis symmetrica hereditaria in Japanese families

INTERNATIONAL JOURNAL OF DERMATOLOGY (2014)

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INTERNATIONAL JOURNAL OF DERMATOLOGY
Volume 53, Issue 3, Pages E194-E196

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WILEY
DOI: 10.1111/j.1365-4632.2012.05765.x

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Dermatology

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