A Natural History Study of Timothy Syndrome.

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Bibliographic Details
Title: A Natural History Study of Timothy Syndrome.
Authors: Timothy KW; The Timothy Syndrome Foundation, Charitable Organization, Brigham City, UT, USA., Bauer R; Laboratory of Biochemistry and Genetics, National Institute of Diabetes, Digestive, and Kidney Diseases, National Institute of Health, Bethesda, MD, USA.; Division of Endocrinology, Metabolism, and Molecular Medicine, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA., Larkin KA; Laboratory of Biochemistry and Genetics, National Institute of Diabetes, Digestive, and Kidney Diseases, National Institute of Health, Bethesda, MD, USA.; Department of Cell Biology, Yale School of Medicine, 295 Congress Ave, New Haven, CT, USA., Walsh EP; Department of Cardiology, Harvard Medical School, Boston Children's Hospital, Boston, MA, USA., Abrams DJ; Department of Cardiology, Harvard Medical School, Boston Children's Hospital, Boston, MA, USA., Gonzalez Corcia C; Department of Cardiology, Sainte Justine Hospital, Montreal, QC, Canada., Valsamakis A; Clinical Development and Medical Affairs, Roche Diagnostics Solutions, Pleasanton, CA, USA., Pitt GS; Cardiovascular Research Institute, Weill Cornell Medicine, New York, NY, USA., Dick IE; Department of Physiology, School of Medicine, University of Maryland, Baltimore, MD, USA. ied@som.umaryland.edu., Golden A; Laboratory of Biochemistry and Genetics, National Institute of Diabetes, Digestive, and Kidney Diseases, National Institute of Health, Bethesda, MD, USA.
Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2024 Nov 23; Vol. 19 (1), pp. 433. Date of Electronic Publication: 2024 Nov 23.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural
Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE
Database: MEDLINE Ultimate
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Description
ISSN:1750-1172
DOI:10.1186/s13023-024-03445-x