CNS demyelination in fibrodysplasia ossificans progressiva

Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder of progressive heterotopic ossification (HO) caused by a recurrent activating mutation of ACVR1/ALK2, a bone morphogenetic protein (BMP) type I receptor. FOP is characterized by progressive HO, which is associated with inflammati...

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Hauptverfasser: Kan, Lixin, Kitterman, Joseph A., Procissi, Daniele, Chakkalakal, Salin, Peng, Chian-Yu, McGuire, Tammy L., Goldsby, Robert E., Pignolo, Robert J., Shore, Eileen M., Kaplan, Frederick S., Kessler, John A.
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2012
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Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3894630/
https://ncbi.nlm.nih.gov/pubmed/22736080
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00415-012-6563-x
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