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Evaluating the mutational spectrum of SIN3A alterations: a case series of patients profiled by next generation sequencing

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Year: 2021
Type: article
Source: Molecular Genetics and Metabolism
DOI: 10.1016/s1096-7192(21)00501-1
Authors: Scott Hickey, Dennis Bartholomew, Kristen Truxal, Kim McBride, Kandamurugu Manickam, Mari Mori, Don Corsmeier, Vijayakumar Jayaraman, Ashita Dave-Wala, Aimee McKinney, Amy Wetzel, Saranga Wijeratne, Valentina Caceres, Shannon Garner, Sayaka Hashimoto, Theodora Matthews, Danielle Mouhlas, Maggie Humphrey, Tom Grossman, Benjamin Kelly, Daniel Koboldt, Vincent Magrini, Peter White, Richard Wilson, Catherine Cottrell, Kristy Lee, Mariam Mathew, Marilena Melas
Language: English

Topic: Genomics and Rare Diseases
Subfield: Genetics
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed
OpenAlex ID: W3152669685
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Related to: 10
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