| 1 | AMT, GLDC, NKH1, NKH2
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| Recurrent mutations in p- and t-proteins of the glycine cleavage complex and a novel t-protein mutation (n145i): a strategy for the molecular investigation of patients with nonketotic hyperglycinemia (nkh).
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| Toone JR, Applegarth DA, Coulter-Mackie MB, James ER.
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| Mol Genet Metab 72(4):322-5. 2001
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| 2 | AMT, NKH2
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| A missense mutation (His42Arg) in the T-protein gene from a large Israeli-Arab kindred with nonketotic hyperglycinemia.
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| Kure S, et al.
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| Hum Genet 102 : 430-434. 1998
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| 3 | AMT, NKH2
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| Structure and chromosomal localization of the aminomethyltransferase gene (AMT).
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| Nanao K, et al.
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| Genomics 19 : 27-30. 1994
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| 4 | NKH1, AMT, NKH2
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| Identification of the mutations in the T-protein gene causing typical and atypical nonketotic hyperglycinemia.
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| Nanao K, et al.
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| Hum Genet 93 : 655-658. 1994
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| 5 | NKH1, NKH2
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| Non-ketotic hyperglycinaemia : molecular lesion, diagnosis and pathophysiology.
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| Tada K, et al.
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| J Inherit Metab Dis 16 : 691-703. 1993
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