Associated Papers
RET mutation p.S891A in a Chinese family with familial medullary thyroid carcinoma and associated cutaneous amyloidosis binding OSMR variant p.G513D.
Qi XP et al.
Oncotarget, 2015
A novel missense mutation in oncostatin M receptor beta causing primary localized cutaneous amyloidosis.
Saeedi M et al.
Biomed Research International, 2014
Familial primary localized cutaneous amyloidosis with an oncostatin M receptor-β mutation, Pro694Leu.
Schreml S et al.
Clinical and Experimental Dermatology, 2013
A new c.1845A→T of oncostatin M receptor-β mutation and slightly enhanced oncostatin M receptor-β expression in a Chinese family with primary localized cutaneous amyloidosis.
Wang WH et al.
European Journal of Dermatology : Ejd, 0
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