Human genetics and molecular genomics of Chiari malformation type 1.

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Bibliographic Details
Title: Human genetics and molecular genomics of Chiari malformation type 1.
Authors: Mekbib KY; Department of Neurosurgery, Yale University School of Medicine, New Haven, CT, USA; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA; Harvard Center for Hydrocephalus and Neurodevelopmental Disorders, Massachusetts General Hospital, Boston, MA, USA., Muñoz W; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA; Harvard Center for Hydrocephalus and Neurodevelopmental Disorders, Massachusetts General Hospital, Boston, MA, USA., Allington G; Department of Pathology, Yale University School of Medicine, New Haven, CT, USA., McGee S; GeneDx, Gaithersburg, MD, USA., Mehta NH; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA., Shofi JP; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA., Fortes C; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA., Le HT; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA., Nelson-Williams C; Department of Genetics, Yale University School of Medicine, New Haven, CT, USA., Nanda P; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA., Dennis E; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA., Kundishora AJ; Department of Neurosurgery, Yale University School of Medicine, New Haven, CT, USA., Khanna A; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA., Smith H; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA., Ocken J; Department of Neurosurgery, Yale University School of Medicine, New Haven, CT, USA., Greenberg ABW; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA., Wu R; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA., Moreno-De-Luca A; Department of Radiology, Autism and Developmental Medicine Institute, Genomic Medicine Institute, Geisinger, Danville, PA, USA., DeSpenza T Jr; Department of Neurosurgery, Yale University School of Medicine, New Haven, CT, USA., Zhao S; Department of Genetics, Washington University School of Medicine, St. Louis, MO, USA., Marlier A; Altos Labs, San Diego, CA, USA., Jin SC; Department of Genetics, Washington University School of Medicine, St. Louis, MO, USA; Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, USA., Alper SL; Division of Nephrology and Vascular Biology Research Center, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA; Department of Medicine, Harvard Medical School, Boston, MA, USA., Butler WE; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA., Kahle KT; Department of Neurosurgery, Massachusetts General Hospital, Boston, MA, USA; Harvard Center for Hydrocephalus and Neurodevelopmental Disorders, Massachusetts General Hospital, Boston, MA, USA; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, USA; Broad Institute of MIT and Harvard, Cambridge, MA, USA. Electronic address: kahle.kristopher@mgh.harvard.edu.
Source: Trends in molecular medicine [Trends Mol Med] 2023 Dec; Vol. 29 (12), pp. 1059-1075. Date of Electronic Publication: 2023 Oct 04.
Publication Type: Journal Article; Review
Journal Info: Publisher: Elsevier Science Ltd Country of Publication: England NLM ID: 100966035 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1471-499X (Electronic) Linking ISSN: 14714914 NLM ISO Abbreviation: Trends Mol Med Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1471-499X
DOI:10.1016/j.molmed.2023.08.013