KVLQT1, the rhythm of imprinting
- PMID: 9020829
- DOI: 10.1038/ng0297-113
KVLQT1, the rhythm of imprinting
Comment on
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Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.Nat Genet. 1997 Feb;15(2):181-5. doi: 10.1038/ng0297-181. Nat Genet. 1997. PMID: 9020845
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A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome.Nat Genet. 1997 Feb;15(2):186-9. doi: 10.1038/ng0297-186. Nat Genet. 1997. PMID: 9020846
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Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.Nat Genet. 1997 Feb;15(2):181-5. doi: 10.1038/ng0297-181. Nat Genet. 1997. PMID: 9020845
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