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Showing results for: AUTHOR - Abbott, K

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Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder Hum Mol Genet - 2015-04-01 Kumar, R; Corbett, MA; Smith, NJ; Jolly, LA; Tan, C; Keating, DJ; Duffield, MD; Utsumi, T; Moriya, K; Smith, KR; Hoischen, A; Abbott, K; Harbord, MG; Compton, AG; Woenig, JA; Arts, P; Kwint, M; Wieskamp, N; Gijsen, S; Veltman, JA; Bahlo, M; Gleeson, JG; Haan, E; Gecz, J
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