Human pathology

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PEXs

Members

- PEX1
- PEX2
- PEX3
- PEX4
- PEX5
- PEX6
- PEX7 - peroxin-7 - mutations in Refsum disease and rhizomelic chondrodysplasia punctata type 1
- PEX8
- PEX9
- PEX10 - peroxin-10 (MIM.602859) - Zelleweger?s syndrome complementation group 7, neonatal adrenoleukodystrophy
- PEX11
- PEX12
- PEX13
- PEX14
- PEX15
- PEX16
- PEX17
- PEX18
- PEX19
- PEX20
- PEX21
- PEX22
- PEX23
- PEX24
- PEX25
- PEX26 - peroxin-26 - peroxisome-biogenesis disorders complementation group 8
- PEX27
- PEX28
- PEX29