HuGE Literature Finder
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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, |
Targeted sequencing and identification of genetic variants in sporadic inclusion body myositis. Neuromuscular disorders : NMD 2015 Apr 25 (4): 289-96. Weihl Conrad C, Baloh Robert H, Lee Youjin, Chou Tsui-Fen, Pittman Sara K, Lopate Glenn, Allred Peggy, Jockel-Balsarotti Jennifer, Pestronk Alan, Harms Matthew |
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- Page last updated:Jun 28, 2022
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