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