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Oxford University Press

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N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratoderma

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Sequential deletion of C-terminal amino acids of the E 1 α component of the pyruvate dehydrogenase (PDH) complex leads to reduced steady-state levels of functional E 1 α 2 β 2 tetramers: implications for patients with PDH deficiency

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Promoter-Dependent Activity on Androgen Receptor N-Terminal Domain Mutations in Androgen Insensitivity Syndrome

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