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Institution Date Title Author
臺大學術典藏 2020-11-03T11:32:32Z Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4) gene Houlden H.; Salih M.A.M.; Timmerman V.; de Jonghe P.; Auer-Grumbach M.; Di Maria E.; Scaravilli F.; Wood N.W.; Reilly M.M.; Davis M.B.; An S.-F.; Sweeney M.G.; Groves M.J.; Stephenson D.A.; MING-JEN LEE
臺大學術典藏 2020-03-03T02:33:36Z Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4) gene MING-JEN LEE; Stephenson D.A.; Groves M.J.; Sweeney M.G.; Davis M.B.; An S.-F.; Houlden H.; Salih M.A.M.; Timmerman V.; de Jonghe P.; Auer-Grumbach M.; Di Maria E.; Scaravilli F.; Wood N.W.; Reilly M.M.
臺大學術典藏 2020-03-03T02:33:36Z Mutation of the sterol 27-hydroxylase gene (CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosis [4] MING-JEN LEE; Huang Y.-C.; Sweeney M.G.; Wood N.W.; Reilly M.M.; Yip P.-K.
臺大學術典藏 2020-03-03T02:33:36Z Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth disease MING-JEN LEE; Nelson I.; Houlden H.; Sweeney M.G.; Hilton-Jones D.; Blake J.; Wood N.W.; Reilly M.M.
臺大學術典藏 2002 Mutation of the sterol 27-hydroxylase gene (CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosis [4] Yip P.-K.; Reilly M.M.; Wood N.W.; Sweeney M.G.; Huang Y.-C.; MING-JEN LEE

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