DHDPSL
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| dihydrodipicolinate synthase-like, mitochondrial | |
|---|---|
| Identifiers | |
| Symbol | DHDPSL |
| Alt. symbols | C10orf65 |
| Entrez | 112817 |
| HUGO | 25155 |
| OMIM | 613597 |
| RefSeq | NM_138413 |
| Other data | |
| Locus | Chr. 10 q24.1 |
DHDPSL is a human gene.
Defects can be associated with primary hyperoxaluria type III.[1]
References
- ↑ Belostotsky R, Seboun E, Idelson GH, et al. (September 2010). "Mutations in DHDPSL are responsible for primary hyperoxaluria type III". Am. J. Hum. Genet. 87 (3): 392–9. doi:10.1016/j.ajhg.2010.07.023. PMC 2933339. PMID 20797690.
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