Long-term survival of neonatal mitochondrial complex III deficiency associated with a novel BCS1L gene mutation.
about
Differential proteomic profiling unveils new molecular mechanisms associated with mitochondrial complex III deficiency.Inhibition of glucose-6-phosphate dehydrogenase sensitizes cisplatin-resistant cells to death.The power of yeast to model diseases of the powerhouse of the cell.Mitochondrial disorders caused by mutations in respiratory chain assembly factors.Nuclear gene mutations as the cause of mitochondrial complex III deficiencyHigh incidence and variable clinical outcome of cardiac hypertrophy due to ACAD9 mutations in childhood.Clinical and biochemical features associated with BCS1L mutation.Human diseases associated with defects in assembly of OXPHOS complexes
P2860
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P2860
Long-term survival of neonatal mitochondrial complex III deficiency associated with a novel BCS1L gene mutation.
description
2010 nî lūn-bûn
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2010年の論文
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2010年学术文章
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2010年学术文章
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2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
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2010年學術文章
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name
Long-term survival of neonatal ...... h a novel BCS1L gene mutation.
@en
Long-term survival of neonatal ...... h a novel BCS1L gene mutation.
@nl
type
label
Long-term survival of neonatal ...... h a novel BCS1L gene mutation.
@en
Long-term survival of neonatal ...... h a novel BCS1L gene mutation.
@nl
prefLabel
Long-term survival of neonatal ...... h a novel BCS1L gene mutation.
@en
Long-term survival of neonatal ...... h a novel BCS1L gene mutation.
@nl
P2093
P50
P1476
Long-term survival of neonatal ...... h a novel BCS1L gene mutation.
@en
P2093
Birgit Czermin
Douglass M Turnbull
Francesca Meloni
Helen A L Tuppen
Iliana Ferrero
Janev Fehmi
Langping He
Robert McFarland
Robert W Taylor
P304
P356
10.1016/J.YMGME.2010.04.010
P577
2010-04-24T00:00:00Z