Genomic and biochemical analysis of repeatedly observed variants in DBT in individuals with maple syrup urine disease of Central American ancestry.

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Bibliographic Details
Title: Genomic and biochemical analysis of repeatedly observed variants in DBT in individuals with maple syrup urine disease of Central American ancestry.
Authors: Billington CJ Jr; Children's National Rare Disease Institute, Washington, District of Columbia, USA.; Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota, USA., Chapman KA; Children's National Rare Disease Institute, Washington, District of Columbia, USA., Leon E; Children's National Rare Disease Institute, Washington, District of Columbia, USA., Meltzer BW; Laboratory Medicine, Children's National Hospital, Washington, District of Columbia, USA., Berger SI; Children's National Rare Disease Institute, Washington, District of Columbia, USA., Olson M; HemoShear Therapeutics, Inc., Charlottesville, Virginia, USA., Figler RA; HemoShear Therapeutics, Inc., Charlottesville, Virginia, USA., Hoang SA; HemoShear Therapeutics, Inc., Charlottesville, Virginia, USA., Wanxing C; Georgetown University Hospital, Washington, District of Columbia, USA., Wamhoff BR; HemoShear Therapeutics, Inc., Charlottesville, Virginia, USA., Collado MS; HemoShear Therapeutics, Inc., Charlottesville, Virginia, USA., Cusmano-Ozog K; Department of Pathology, Stanford University Medical Center, Stanford, California, USA.
Source: American journal of medical genetics. Part A [Am J Med Genet A] 2022 Sep; Vol. 188 (9), pp. 2738-2749. Date of Electronic Publication: 2022 Jul 07.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Database: MEDLINE Ultimate
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