Severe neurological manifestations in an Egyptian patient with a novel frameshift mutation in the Glutaryl-CoA dehydrogenase gene.
about
Severe neurological manifestations in an Egyptian patient with a novel frameshift mutation in the Glutaryl-CoA dehydrogenase gene.
description
2016 nî lūn-bûn
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2016年の論文
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年學術文章
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2016年學術文章
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name
Severe neurological manifestat ...... utaryl-CoA dehydrogenase gene.
@en
Severe neurological manifestat ...... utaryl-CoA dehydrogenase gene.
@nl
type
label
Severe neurological manifestat ...... utaryl-CoA dehydrogenase gene.
@en
Severe neurological manifestat ...... utaryl-CoA dehydrogenase gene.
@nl
prefLabel
Severe neurological manifestat ...... utaryl-CoA dehydrogenase gene.
@en
Severe neurological manifestat ...... utaryl-CoA dehydrogenase gene.
@nl
P2093
P2860
P1476
Severe neurological manifestat ...... utaryl-CoA dehydrogenase gene.
@en
P2093
Ahmed Moseilhy
Allal Ouhtit
Heba S A El Abd
Magdy M Hassan
Rajaa El Bekay
Shaimaa A Mohammad
Ussama M Abdel-Motal
P2860
P2888
P356
10.1007/S11011-016-9879-X
P577
2016-08-01T00:00:00Z