Connection
Sara Miller to Mutation, Missense
This is a "connection" page, showing publications Sara Miller has written about Mutation, Missense.
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0.091 |
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Weihl CC, Miller SE, Zaidman CM, Pestronk A, Baloh RH, Al-Lozi M. Novel GNE mutations in two phenotypically distinct HIBM2 patients. Neuromuscul Disord. 2011 Feb; 21(2):102-5.
Score: 0.074
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Gurnett CA, Desruisseau DM, McCall K, Choi R, Meyer ZI, Talerico M, Miller SE, Ju JS, Pestronk A, Connolly AM, Druley TE, Weihl CC, Dobbs MB. Myosin binding protein C1: a novel gene for autosomal dominant distal arthrogryposis type 1. Hum Mol Genet. 2010 Apr 01; 19(7):1165-73.
Score: 0.017