Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Myositis and SQSTM1[original query] |
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Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis. Neurobiology of aging 2016 Nov 47 218.e1-218.e9. Gang Qiang, Bettencourt Conceição, Machado Pedro M, Brady Stefen, Holton Janice L, Pittman Alan M, Hughes Deborah, Healy Estelle, Parton Matthew, Hilton-Jones David, Shieh Perry B, Needham Merrilee, Liang Christina, Zanoteli Edmar, de Camargo Leonardo Valente, De Paepe Boel, De Bleecker Jan, Shaibani Aziz, Ripolone Michela, Violano Raffaella, Moggio Maurizio, Barohn Richard J, Dimachkie Mazen M, Mora Marina, Mantegazza Renato, Zanotti Simona, Singleton Andrew B, Hanna Michael G, Houlden Henry, |
Genetics in inclusion body myositis. Current opinion in rheumatology 2017 8 29 (6): 639-644. Rothwell Simon, Lilleker James B, Lamb Janine |
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- Page last updated:Apr 22, 2024
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