Lack of common mutation in the alfa-subunit of the mitochondrial trifunctional protein and the polymorphism of CYP2E1 in three Japanese women with acute fatty liver of pregnancy/HELLP syndrome
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Observations regarding retinopathy in mitochondrial trifunctional protein deficienciesAcute Fatty Liver Disease of Pregnancy: Updates in Pathogenesis, Diagnosis, and Management.No mutation was found in the alpha-subunit of the mitochondrial tri-functional protein in one patient with severe acute fatty liver of pregnancy and her relatives.
P2860
Lack of common mutation in the alfa-subunit of the mitochondrial trifunctional protein and the polymorphism of CYP2E1 in three Japanese women with acute fatty liver of pregnancy/HELLP syndrome
description
im Dezember 2004 veröffentlichter wissenschaftlicher Artikel
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scientific article published on 01 December 2004
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wetenschappelijk artikel
@nl
наукова стаття, опублікована в грудні 2004
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name
Lack of common mutation in the ...... er of pregnancy/HELLP syndrome
@en
Lack of common mutation in the ...... er of pregnancy/HELLP syndrome
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type
label
Lack of common mutation in the ...... er of pregnancy/HELLP syndrome
@en
Lack of common mutation in the ...... er of pregnancy/HELLP syndrome
@nl
prefLabel
Lack of common mutation in the ...... er of pregnancy/HELLP syndrome
@en
Lack of common mutation in the ...... er of pregnancy/HELLP syndrome
@nl
P2093
P1433
P1476
Lack of common mutation in the ...... er of pregnancy/HELLP syndrome
@en
P2093
Emiko Mikami
Futoshi Nagasaki
Koji Fukushima
Noriatsu Kanno
Tooru Shimosegawa
Yoshiyuki Ueno
Yuki Moritoki
P304
P356
10.1016/J.HEPRES.2004.09.005
P577
2004-12-01T00:00:00Z