Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosis
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Abstract
Primary cutaneous amyloidosis (PCA) is an itchy skin disorder associated with amyloid deposits in the superficial dermis. The disease is relatively common in Southeast Asia and South America. Autosoma...
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European Journal of Human Genetics (2010) 18, 26–32
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