Associated Papers
A novel oncostatin M/interleukin-31 receptor mutation in familial primary localized cutaneous amyloidosis.
Adams R et al.
Clinical and Experimental Dermatology, 2020
The molecular skin pathology of familial primary localized cutaneous amyloidosis.
Tanaka A et al.
Experimental Dermatology, 2010
Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosis.
Lin MW et al.
European Journal of Human Genetics : Ejhg, 2010
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