Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease.
about
An overview of the Prince Salman Center for Disability Research scientific outcomesLarge contiguous gene deletions in Sjögren-Larsson syndromeUpregulation of N-acetylaspartic acid induces oxidative stress to contribute in disease pathophysiology.A thematic review of scientific and family interests in Canavan Disease: where are the developmentalists?A novel syndrome of abnormal striatum and congenital cataract: evidence for linkage to chromosomes 11.Pinar T. Ozand: Clinician-Scientist Extraordinaire.Identification of novel genomic imbalances in Saudi patients with congenital heart disease.Clinical and biochemical features associated with BCS1L mutation.Novel intragenic deletion in OPHN1 in a family causing XLMR with cerebellar hypoplasia and distinctive facial appearance.
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P2860
Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease.
description
2008 nî lūn-bûn
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2008年の論文
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2008年学术文章
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2008年学术文章
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2008年学术文章
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2008年学术文章
@zh-my
2008年学术文章
@zh-sg
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2008年學術文章
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name
Genome-wide gene expression pr ...... patients with Canavan disease.
@en
type
label
Genome-wide gene expression pr ...... patients with Canavan disease.
@en
prefLabel
Genome-wide gene expression pr ...... patients with Canavan disease.
@en
P2093
P2860
P1433
P1476
Genome-wide gene expression pr ...... patients with Canavan disease.
@en
P2093
Ali Al-Odaib
Aziza Chedrawi
Bashayer R Al-Mubarak
Brian F Meyer
Dilek Colak
Faiqa Imtiaz
Fatma Al-Zahrani
Hesham Al-Dhalaan
Moeenaldeen Al-Sayed
Mohammad Al-Owain
P2860
P2888
P304
P356
10.1097/GIM.0B013E31818337A8
P407
P577
2008-09-01T00:00:00Z
P6179
1002691653