Familial primary localized cutaneous amyloidosis with an oncostatin M receptor-ß mutation, Pro694Leu.
Clin Exp Dermatol
; 38(8): 932-5, 2013 Dec.
Article
in En
| MEDLINE
| ID: mdl-23692662
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Mutation, Missense
/
Amyloidosis, Familial
/
Oncostatin M Receptor beta Subunit
Limits:
Adult
/
Female
/
Humans
Language:
En
Journal:
Clin Exp Dermatol
Year:
2013
Document type:
Article
Affiliation country:
Alemania