Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders. | NobleID

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Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders.

NobleID: NI1P54W39R00S69
Persistent link: https://nobleid.org/ark:/48914/w1/20260515/1A3AB2FD

Type:Journal Article

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