Dravet syndrome: new potential genetic modifiers, imaging abnormalities, and ictal findings.
about
Rare variants of small effect size in neuronal excitability genes influence clinical outcome in Japanese cases of SCN1A truncation-positive Dravet syndrome.Pharmacotherapy for Dravet Syndrome.Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms.Dravet Syndrome: Diagnosis and Long-Term Course.Pitfalls in genetic testing: the story of missed SCN1A mutations.Dravet syndrome and its mimics: Beyond SCN1A.Co-occurring malformations of cortical development and SCN1A gene mutations.Mitochondrial respiratory chain defects in skin fibroblasts from patients with Dravet syndrome.
P2860
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P2860
Dravet syndrome: new potential genetic modifiers, imaging abnormalities, and ictal findings.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
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2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh-hant
name
Dravet syndrome: new potential ...... rmalities, and ictal findings.
@en
Dravet syndrome: new potential ...... rmalities, and ictal findings.
@nl
type
label
Dravet syndrome: new potential ...... rmalities, and ictal findings.
@en
Dravet syndrome: new potential ...... rmalities, and ictal findings.
@nl
prefLabel
Dravet syndrome: new potential ...... rmalities, and ictal findings.
@en
Dravet syndrome: new potential ...... rmalities, and ictal findings.
@nl
P2093
P2860
P50
P356
P1433
P1476
Dravet syndrome: new potential ...... rmalities, and ictal findings.
@en
P2093
Ann-Liz Träskelin
Anna-Kaisa Anttonen
Anne Polvi
Eija Gaily
Elina Liukkonen
Kai Eriksson
Markus Lommi
P2860
P304
P356
10.1111/EPI.12256
P577
2013-06-28T00:00:00Z