Familial primary localized cutaneous amyloidosis results from either dominant or recessive mutations in OSMR

Acta Derm Venereol. 2015 Nov;95(8):1005-7. doi: 10.2340/00015555-2104.

Authors

Abdul Wali¹, Lu Liu, Takuya Takeichi, Musharraf Jelani, Obaid Ur Rahman, Yee Kiat Heng, Steven Thng, Joyce Lee, Masashi Akiyama, John A McGrath, Regina C Betz

Affiliation

¹ Institute of Human Genetics, University of Bonn, DE-53127 Bonn, Germany.

PMID: 25792357
DOI: 10.2340/00015555-2104

No abstract available

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Adolescent
Adult
Age of Onset
Aged
Amyloidosis, Familial / genetics*
Exons
Female
Genes, Dominant
Genes, Recessive
Heterozygote
Homozygote
Humans
Male
Middle Aged
Mutation
Oncostatin M Receptor beta Subunit / genetics*
Pedigree
Polymorphism, Single Nucleotide
Skin Diseases, Genetic / genetics*
Young Adult

Substances

OSMR protein, human
Oncostatin M Receptor beta Subunit

Supplementary concepts

Amyloidosis, Primary Cutaneous