Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein (Q34308654)
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(P31) (Q13442814)
(P304) 141-145
(P407) (Q1860)
(P433) 2
(P478) 9
(P577) Wednesday, February 1, 1995
(P921) (Q34956)
(Q7936965)
(P1433) (Q976454)
(P1476) "Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein" (language: en)
(P2093) Ouahchi K
Arita M
Kayden H
Hentati F
Ben Hamida M
Sokol R
Arai H
Inoue K
Mandel JL
Koenig M
(P2860) (Q56609576)
(Q54135322)
(Q38902078)
(Q34345703)
(Q36757666)
(Q28262033)
(Q28131805)
(Q72021754)
(Q69762145)
(Q68772421)
(Q69703003)
(Q70704945)
(Q70409412)
(Q41283841)
(Q34242273)
(Q35827647)
(Q72586488)
(Q70940275)
(Q67956849)
(Q55671005)
(Q37186517)
(Q34324926)
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