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Complex effects on CaV2.1 channel gating caused by a CACNA1A variant associated with a severe neurodevelopmental disorder.

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Title: Complex effects on CaV2.1 channel gating caused by a CACNA1A variant associated with a severe neurodevelopmental disorder.
Authors: Grosso BJ; Departments of Pathology/Biochemistry and Molecular Biology, University of Maryland School of Medicine, 108 North Greene Street, Room 208A, Baltimore, MD, 21201, USA., Kramer AA; Departments of Pathology/Biochemistry and Molecular Biology, University of Maryland School of Medicine, 108 North Greene Street, Room 208A, Baltimore, MD, 21201, USA., Tyagi S; Medical Scientist Training Program, Department of Neurology, Yale School of Medicine, New Haven, CT, 06520, USA., Bennett DF; Departments of Pathology/Biochemistry and Molecular Biology, University of Maryland School of Medicine, 108 North Greene Street, Room 208A, Baltimore, MD, 21201, USA., Tifft CJ; National Institutes of Health Undiagnosed Diseases Program, Common Fund, National Institutes of Health, Bethesda, MD, 20892, USA.; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, 20892, USA., D'Souza P; National Institutes of Health Undiagnosed Diseases Program, Common Fund, National Institutes of Health, Bethesda, MD, 20892, USA., Wangler MF; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA., Macnamara EF; National Institutes of Health Undiagnosed Diseases Program, Common Fund, National Institutes of Health, Bethesda, MD, 20892, USA., Meza U; Department of Physiology and Biophysics, School of Medicine, Autonomous University of San Luis Potosí, Carranza #2405, SLP 78210, San Luis Potosí, Mexico., Bannister RA; Departments of Pathology/Biochemistry and Molecular Biology, University of Maryland School of Medicine, 108 North Greene Street, Room 208A, Baltimore, MD, 21201, USA. rbannister@som.umaryland.edu.; Center for Scientific Review, Division of Neuroscience, Development and Aging, National Institutes of Health, 6701 Rockledge Drive, Bethesda, MD, 20892, USA. rbannister@som.umaryland.edu.
Source: Scientific reports [Sci Rep] 2022 Jun 02; Vol. 12 (1), pp. 9186. Date of Electronic Publication: 2022 Jun 02.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural
Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Complex effects on Ca<subscript>V</subscript>2.1 channel gating caused by a CACNA1A variant associated with a severe neurodevelopmental disorder.
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  Data: <searchLink fieldCode="AU" term="%22Grosso+BJ%22">Grosso BJ</searchLink>; Departments of Pathology/Biochemistry and Molecular Biology, University of Maryland School of Medicine, 108 North Greene Street, Room 208A, Baltimore, MD, 21201, USA.<br /><searchLink fieldCode="AU" term="%22Kramer+AA%22">Kramer AA</searchLink>; Departments of Pathology/Biochemistry and Molecular Biology, University of Maryland School of Medicine, 108 North Greene Street, Room 208A, Baltimore, MD, 21201, USA.<br /><searchLink fieldCode="AU" term="%22Tyagi+S%22">Tyagi S</searchLink>; Medical Scientist Training Program, Department of Neurology, Yale School of Medicine, New Haven, CT, 06520, USA.<br /><searchLink fieldCode="AU" term="%22Bennett+DF%22">Bennett DF</searchLink>; Departments of Pathology/Biochemistry and Molecular Biology, University of Maryland School of Medicine, 108 North Greene Street, Room 208A, Baltimore, MD, 21201, USA.<br /><searchLink fieldCode="AU" term="%22Tifft+CJ%22">Tifft CJ</searchLink>; National Institutes of Health Undiagnosed Diseases Program, Common Fund, National Institutes of Health, Bethesda, MD, 20892, USA.; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, 20892, USA.<br /><searchLink fieldCode="AU" term="%22D'Souza+P%22">D'Souza P</searchLink>; National Institutes of Health Undiagnosed Diseases Program, Common Fund, National Institutes of Health, Bethesda, MD, 20892, USA.<br /><searchLink fieldCode="AU" term="%22Wangler+MF%22">Wangler MF</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.<br /><searchLink fieldCode="AU" term="%22Macnamara+EF%22">Macnamara EF</searchLink>; National Institutes of Health Undiagnosed Diseases Program, Common Fund, National Institutes of Health, Bethesda, MD, 20892, USA.<br /><searchLink fieldCode="AU" term="%22Meza+U%22">Meza U</searchLink>; Department of Physiology and Biophysics, School of Medicine, Autonomous University of San Luis Potosí, Carranza #2405, SLP 78210, San Luis Potosí, Mexico.<br /><searchLink fieldCode="AU" term="%22Bannister+RA%22">Bannister RA</searchLink>; Departments of Pathology/Biochemistry and Molecular Biology, University of Maryland School of Medicine, 108 North Greene Street, Room 208A, Baltimore, MD, 21201, USA. rbannister@som.umaryland.edu.; Center for Scientific Review, Division of Neuroscience, Development and Aging, National Institutes of Health, 6701 Rockledge Drive, Bethesda, MD, 20892, USA. rbannister@som.umaryland.edu.
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