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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
KVLQT1, the rhythm of imprinting.
Mannens M, Wilde A.
Mannens M, et al.
Nat Genet. 1997 Feb;15(2):113-5. doi: 10.1038/ng0297-113.
Nat Genet. 1997.
PMID: 9020829
No abstract available.
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A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome.
Neyroud N, Tesson F, Denjoy I, Leibovici M, Donger C, Barhanin J, Fauré S, Gary F, Coumel P, Petit C, Schwartz K, Guicheney P.
Neyroud N, et al.
Nat Genet. 1997 Feb;15(2):186-9. doi: 10.1038/ng0297-186.
Nat Genet. 1997.
PMID: 9020846
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