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Year | Number of Results |
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1998 | 1 |
2003 | 1 |
2024 | 0 |
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Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndrome.
Pediatr Res. 2003 May;53(5):744-8. doi: 10.1203/01.PDR.0000059750.17002.B6. Epub 2003 Mar 5.
Pediatr Res. 2003.
PMID: 12621127
Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome.
Itoh T, Tanaka T, Nagai R, Kamiya T, Sawayama T, Nakayama T, Tomoike H, Sakurada H, Yazaki Y, Nakamura Y.
Itoh T, et al.
Hum Genet. 1998 Apr;102(4):435-9. doi: 10.1007/s004390050717.
Hum Genet. 1998.
PMID: 9600240
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