Condition: PEROXISOME BIOGENESIS DISORDER 11B
rs61752115
in
PEX13
gene and
PEROXISOME BIOGENESIS DISORDER 11B
PMID 10332040
1999 Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders.
PMID 10441568
1999 PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders.