| 1 | CTH, CTHD
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| Ancient origin of the CTH alelle carrying the c.200C>T (p.T67I) variant in patients with cystathioninuria.
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| Espinós C, García-Cazorla A, Martínez-Rubio D, Martínez-Martínez E, Vilaseca MA, Pérez-Dueñas B, Kožich V, Palau F, Artuch R.
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| Clin Genet 78(6):554-9. doi: 10.1111/j.1399-0004.2010.01431.x.
2010
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| 2 | CTH, CTHD
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| Cystathionine gamma-lyase deficiency and overproliferation of smooth muscle cells.
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| Yang G, Wu L, Bryan S, Khaper N, Mani S, Wang R.
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| Cardiovasc Res 86(3):487-95. Epub 2010 Jan 5.
2010
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| 3 | CTH, CTHD
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| Cystathionine gamma-lyase: Clinical, metabolic, genetic, and structural studies.
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| Kraus JP, Hasek J, Kozich V, Collard R, Venezia S, Janosíková B, Wang J, Stabler SP, Allen RH, Jakobs C, Finn CT, Chien YH, Hwu WL, Hegele RA, Mudd SH.
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| Mol Genet Metab 97(4):250-9. Epub 2009 Apr 9.
2009
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| 4 | CTH, CTHD
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| Genomic basis of cystathioninuria (MIM 219500) revealed by multiple mutations in cystathionine gamma-lyase (CTH).
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| Wang J, Hegele RA.
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| Hum Genet 112(4):404-8. Epub 2003 Feb 6. 2003
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| 5 | CTHD
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| Cystathioninuria: nature of the defect.
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| Frimpter GW.
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| Science 149 : 1095-1096. 1965
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