| 1 | ITGA7, ITGA7D, LVNC13, MYH7B
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| Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy.
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| Esposito T, Sampaolo S, Limongelli G, Varone A, Formicola D, Diodato D, Farina O, Napolitano F, Pacileo G, Gianfrancesco F, Di Iorio G.
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| Orphanet J Rare Dis 8:91. doi: 10.1186/1750-1172-8-91.
2013
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| 2 | FKRP, FKTN, ITGA7, ITGA7D, LAMA2, MDC1A, MDC1B, POMGNT1, POMT1, RSMD1, SEPN1, WLKWS1, WLKWS4
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| Case 35-2006 -- A Newborn Boy with Hypotonia.
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| Brown RH Jr, Grant PE, Pierson CR.
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| N Engl J Med 355(20):2132-2142. No abstract available. 2006
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| 3 | ITGA7, ITGA7D
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| Mutations in the integrin alpha7 gene cause congenital myopathy.
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| Hayashi YK, et al.
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| Nat Genet 19 : 94-97. 1998
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| 4 | ITGA7, ITGA7D
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| Absence of integrin alpha 7 causes a novel form of muscular dystrophy.
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| Mayer U, Saher G, Fassler R, Bornemann A, Echtermeyer F, von der Mark H, Miosge N, Poschl E, von der Mark K.
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| Nat Genet 17(3):318-23. 1997
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