| 1 | TAZ, DTNA, INVM, LVNC
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| Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, alpha-dystrobrevin and FK Binding Protein-12.
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| Kenton AB, Sanchez X, Coveler KJ, Makar KA, Jimenez S, Ichida F, Murphy RT, Elliott PM, McKenna W, Bowles NE, Towbin JA, Bowles KR.
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| Mol Genet Metab 82(2):162-6. 2004
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| 2 | INVM, TAZ
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| Mutation analysis of the G4.5 gene in patients with isolated left ventricular noncompaction.
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| Chen R, Tsuji T, Ichida F, Bowles KR, Yu X, Watanabe S, Hirono K, Tsubata S, Hamamichi Y, Ohta J, Imai Y, Bowles NE, Miyawaki T, Towbin JA.
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| Mol Genet Metab 77(4):319-25. 2002
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| 3 | INVM
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| Xq28-linked noncompaction of the left ventricular myocardium: prenatal diagnosis and pathologic analysis of affected individuals.
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| Bleyl SB, Mumford BR, Brown-Harrison MC, Pagotto LT, Carey JC, Pysher TJ, Ward K, Chin TK.
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| Am J Med Genet 72(3):257-65. 1997
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| 4 | CMD3A, BTHS, INVM, TAZ
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| The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies.
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| D'Adamo P, Fassone L, Gedeon A, Janssen EA, Bione S, Bolhuis PA, Barth PG, Wilson M, Haan E, Orstavik KH, Patton MA, Green AJ, Zammarchi E, Donati MA, Toniolo D.
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| Am J Hum Genet 61(4):862-7. 1997
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| 5 | INVM, TAZ
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| Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome.
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| Bleyl SB, Mumford BR, Thompson V, Carey JC, Pysher TJ, Chin TK, Ward K.
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| Am J Hum Genet 61(4):868-72. 1997
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