DHDPSL

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

  1. ↑ 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 2933339Freely accessible. PMID 20797690.


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