Clinical and genetic analysis of long QT syndrome in children from six families in Saudi Arabia: are they different?
about
Congenital Long QT Syndrome: An Update and Present Perspective in Saudi Arabia.Genotype-phenotype analysis of Jervell and Lange-Nielsen syndrome in six families from Saudi Arabia.Recurrent and Founder Mutations in the Netherlands: the Long-QT Syndrome.Inhibition of nonsense-mediated mRNA decay by antisense morpholino oligonucleotides restores functional expression of hERG nonsense and frameshift mutations in long-QT syndromeLong QT syndrome mutation detection by SNaPshot technique.
P2860
Clinical and genetic analysis of long QT syndrome in children from six families in Saudi Arabia: are they different?
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2009 nî lūn-bûn
@nan
2009 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Clinical and genetic analysis ...... di Arabia: are they different?
@ast
Clinical and genetic analysis ...... di Arabia: are they different?
@en
type
label
Clinical and genetic analysis ...... di Arabia: are they different?
@ast
Clinical and genetic analysis ...... di Arabia: are they different?
@en
prefLabel
Clinical and genetic analysis ...... di Arabia: are they different?
@ast
Clinical and genetic analysis ...... di Arabia: are they different?
@en
P2093
P2860
P1433
P1476
Clinical and genetic analysis ...... di Arabia: are they different?
@en
P2093
Ayman S Al-Khadra
Khalaf Al-Khalaf
Marcel M A M Mannens
Safar Al-Shahrani
Saleh Al-Ghamdi
Tarek S Momenah
Zahurul A Bhuiyan
P2860
P2888
P304
P356
10.1007/S00246-008-9377-Y
P577
2009-01-30T00:00:00Z
P5875
P6179
1004303849