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Novel KCNQ1 and HERG missense mutations in Dutch long-QT families
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instance of
scholarly article
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title
Novel KCNQ1 and HERG missense mutations in Dutch long-QT families
(English)
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author name string
R J Jongbloed
series ordinal
1
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A A Wilde
series ordinal
2
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J L Geelen
series ordinal
3
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P Doevendans
series ordinal
4
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C Schaap
series ordinal
5
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I Van Langen
series ordinal
6
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J P van Tintelen
series ordinal
7
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J M Cobben
series ordinal
8
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G C Beaufort-Krol
series ordinal
9
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J P Geraedts
series ordinal
10
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H J Smeets
series ordinal
11
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language of work or name
English
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publication date
1999
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published in
Human Mutation
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volume
13
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issue
4
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page(s)
301-10
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cites work
Missense mutation in the pore region of HERG causes familial long QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C301%3A%3AAID-HUMU7%3E3.0.CO%3B2-V
retrieved
21 January 2018
Mutation of the gene for IsK associated with both Jervell and Lange-Nielsen and Romano-Ward forms of Long-QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C301%3A%3AAID-HUMU7%3E3.0.CO%3B2-V
retrieved
21 January 2018
The long QT syndrome in children. An international study of 287 patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C301%3A%3AAID-HUMU7%3E3.0.CO%3B2-V
retrieved
21 January 2018
The long QT syndrome. Prospective longitudinal study of 328 families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C301%3A%3AAID-HUMU7%3E3.0.CO%3B2-V
retrieved
21 January 2018
A recessive variant of the Romano-Ward long-QT syndrome?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C301%3A%3AAID-HUMU7%3E3.0.CO%3B2-V
retrieved
21 January 2018
Diagnostic criteria for the long QT syndrome. An update
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C301%3A%3AAID-HUMU7%3E3.0.CO%3B2-V
retrieved
21 January 2018
Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291098-1004%281999%2913%3A4%3C301%3A%3AAID-HUMU7%3E3.0.CO%3B2-V
retrieved
21 January 2018
Identifiers
DOI
10.1002/(SICI)1098-1004(1999)13:4<301::AID-HUMU7>3.0.CO;2-V
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PubMed ID
10220144
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