| 1 | DFNA1
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| Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypes.
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| Bom SJ, Kunst HP, Huygen PL, Cremers FP, Cremers CW.
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| Br J Audiol 33(5):335-48. 1999
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| 2 | DFNA1, DIAPH2
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| p140mDia, a mammalian homolog of Drosophila diaphanous, is a target protein for Rho small GTPase and is a ligand for profilin.
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| Watanabe N, Madaule P, Reid T, Ishizaki T, Watanabe G, Kakizuka A, Saito Y, Nakao K, Jockusch BM, Narumiya S.
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| EMBO J 16(11):3044-56. 1997
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| 3 | DFNA1, DIAPH2
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| Rho effectors and reorganization of actin cytoskeleton.
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| Narumiya S, Ishizaki T, Watanabe N.
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| FEBS Lett 410(1):68-72. 1997
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| 4 | DFNA1, DIAPH1, DIAPH2, PCDHGC3
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| Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous.
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| Lynch ED, Lee MK, Morrow JE, Welcsh PL, Leon PE, King MC.
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| Science 278(5341):1315-8. 1997
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| 5 | DFNA1, DIAPH2
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| Diaphanous is required for cytokinesis in Drosophila and shares domains of similarity with the products of the limb deformity gene.
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| Castrillon DH, et al.
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| Development 120 : 3367-3377. 1994
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| 6 | DFNA1, DIAPH1
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| The gene for an inherited form of deafness maps to chromosome 5q31.
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| Leon PE, Raventos H, Lynch E, Morrow J, King MC.
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| Proc Natl Acad Sci U S A 89(11):5181-4. 1992
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| 7 | DFNA1
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| Low frequency hereditary deafness in man with childhood onset.
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| Leon PE, et al.
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| Am J Hum Genet 33 : 209-214. 1981
|