Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders (Q28256545)
scientific article published in December 1997
Language:
(P31) (Q13442814)
(P50) (Q69376172)
(P304) 449-452
(P407) (Q1860)
(P433) 4
(P478) 17
(P577) Monday, December 1, 1997
(P1433) (Q976454)
(P1476) "Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders" (language: en)
(P2093) Portsteffen H
Beyer A
Becker E
Epplen C
Kunau WH
Dodt G
(P2860) (Q24561552)
(Q71700951)
(Q44793813)
(Q54242010)
(Q40914795)
(Q27930969)
(Q36234864)
(Q28295702)
(Q41615832)
(Q25938991)
(Q27860600)
(Q24323901)
(Q24681727)
(Q33862158)
(Q28207783)
(Q41506669)
(Q24314366)
(Q24311431)
(Q61822513)
(Q24311606)
(Q41529353)
(Q27861086)
other details
description scientific article published in December 1997

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