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Pathogenic KCNH2 variant in monozygotic twins with speech delay and lower risk type 2 long QT syndrome.

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Bibliographic Details
Title: Pathogenic KCNH2 variant in monozygotic twins with speech delay and lower risk type 2 long QT syndrome.
Authors: Margiotti K; Human Genetics Lab, Altamedica Main Centre, Viale Liegi 45, Rome, 00198, Italy. katia.margiotti@artemisia.it., Fabiani M; Human Genetics Lab, Altamedica Main Centre, Viale Liegi 45, Rome, 00198, Italy., Zangheri C; Human Genetics Lab, Altamedica Main Centre, Viale Liegi 45, Rome, 00198, Italy., Cima A; Human Genetics Lab, Altamedica Main Centre, Viale Liegi 45, Rome, 00198, Italy., Monaco F; Human Genetics Lab, Altamedica Main Centre, Viale Liegi 45, Rome, 00198, Italy., Libotte F; Human Genetics Lab, Altamedica Main Centre, Viale Liegi 45, Rome, 00198, Italy., Ali' C; Human Genetics Lab, Altamedica Main Centre, Viale Liegi 45, Rome, 00198, Italy., Barone MA; Human Genetics Lab, Altamedica Main Centre, Viale Liegi 45, Rome, 00198, Italy., Viola A; Human Genetics Lab, Altamedica Main Centre, Viale Liegi 45, Rome, 00198, Italy., Mesoraca A; Human Genetics Lab, Altamedica Main Centre, Viale Liegi 45, Rome, 00198, Italy., Giorlandino C; Human Genetics Lab, Altamedica Main Centre, Viale Liegi 45, Rome, 00198, Italy.; Department of Prenatal Diagnosis, Fetal-Maternal Medical Centre, Viale Liegi 45, Altamedica, Rome, 00198, Italy.
Source: Neurogenetics [Neurogenetics] 2025 Aug 15; Vol. 26 (1), pp. 63. Date of Electronic Publication: 2025 Aug 15.
Publication Type: Journal Article; Case Reports
Journal Info: Publisher: Springer-Verlag Country of Publication: United States NLM ID: 9709714 Publication Model: Electronic Cited Medium: Internet ISSN: 1364-6753 (Electronic) Linking ISSN: 13646745 NLM ISO Abbreviation: Neurogenetics Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1364-6753
DOI:10.1007/s10048-025-00842-7