00745nam0-22002771i-450-990000087150403321000008715FED01000008715(Aleph)000008715FED0100000871520011111d--------km-y0itay50------baitay-------001yyAide-mémorie de physique industriellenotes et formulesEd. Lelaurin.ParisE. Bernard et C.1891184 p., 4 tav.ill.17 cmFisica tecnica621Lelaurin,E.ITUNINARICAUNIMARCBK99000008715040332113 AR 14 A 064705FINBCFINBCUNINAING0102534nam 2200457z- 450 991055722310332120211118(CKB)5400000000041713(oapen)https://directory.doabooks.org/handle/20.500.12854/73676(oapen)doab73676(EXLCZ)99540000000004171320202111d2020 |y 0engurmn|---annantxtrdacontentcrdamediacrrdacarrierApplying Next Generation Sequencing and Transgenic Models to Rare Disease ResearchFrontiers Media SA20201 online resource (119 p.)2-88963-524-4 A rare disease is a disease that occurs infrequently in the general population, typically affecting fewer than 200,000 Americans at any given time. More than 30 million people in the United States of America (USA) and 350 million people globally suffer from rare diseases. Out of the 7000+ known rare diseases, less than 5% have approved treatments. Rare diseases are frequently chronic, progressive, degenerative, and life-threatening, compromising the lives of patients by loss of autonomy. In the USA, it can take years for a rare disease patient to receive a correct diagnosis. The socioeconomic burden for rare disease is huge. For those living with diagnosed rare diseases, there is no support system or resource bank for navigating financial, educational, or other aspects of having a rare disease. The purpose of this Research Topic is to bring together leading researchers, non-profit organizations, healthcare providers/diagnostic companies, and pharma/biotech/CROs in the field to provide a broad perspective on the latest advances, challenges, and opportunities in rare disease research.Medical geneticsbicsscScience: general issuesbicsscgenetic analysisGenomicsNext generation sequencingRare diseasetransgenicMedical geneticsScience: general issuesGouw Arvin Medt1317941Jaishankar AmrithaedtBrooks George AedtGouw Arvin MothJaishankar AmrithaothBrooks George AothBOOK9910557223103321Applying Next Generation Sequencing and Transgenic Models to Rare Disease Research3033116UNINA