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Human Molecular Genetics, Vol. 8, Iss. 9, 1999-09 ,pp. : 1631-1636

Oxford University Press

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ATP2A2 mutations in Darier’s disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class

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Human Molecular Genetics, Vol. 8, Iss. 9, 1999-09 ,pp. : 1621-1630

Oxford University Press

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Hailey–Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca 2+ pump

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Transcription factor MEF2A mutations in patients with coronary artery disease

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Evolution of Crohn’s disease-associated Nod2 mutations

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Immunogenetics, Vol. 60, Iss. 2, 2008-02 ,pp. : 115-120

Springer Publishing Company

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