DHDPSL

DHDPSL
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. PMID 20797690. http://linkinghub.elsevier.com/retrieve/pii/S0002-9297(10)00380-0.