Leprecan
| leucine proline-enriched proteoglycan (leprecan) 1 | |
|---|---|
| Identifiers | |
| Symbol | LEPRE1 |
| Entrez | 64175 |
| HUGO | 19316 |
| OMIM | 610339 |
| RefSeq | NM_022356 |
| UniProt | Q32P28 |
| Other data | |
| Locus | Chr. 1 p34.1 |
Leprecan is a protein associated with osteogenesis imperfecta[1] type VIII.
References
- ↑ Cabral WA, Chang W, Barnes AM, et al. (March 2007). "Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta". Nat. Genet. 39 (3): 359–65. PMID 17277775. doi:10.1038/ng1968.
External links
- leprecan protein, human at the US National Library of Medicine Medical Subject Headings (MeSH)
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