GJA1 wt Allele

Known as: HLHS1, Gap Junction Protein, Alpha 1, 43kDa (Connexin 43) Gene, HSS 
Human GJA1 wild-type allele is located in the vicinity of 6q22.31 and is approximately 14 kb in length. This allele, which encodes gap junction alpha… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1986-2016
051019862016

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2011
2011
Oculodentodigital dysplasia (ODDD) is primarily an autosomal dominant human disease caused by any one of over 60 mutations in the… (More)
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2008
Highly Cited
2008
Oculodentodigital dysplasia (ODDD) is a dominant negatively inherited disorder with variable but characteristic anomalies of the… (More)
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2007
2007
Oculodentodigital dysplasia (ODDD) is a dominantly inherited human disorder associated with different symptoms like craniofacial… (More)
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2007
2007
Oculo-dento-digital dysplasia (ODDD, OMIM no.164210) is a pleiotropic disorder caused by mutations in the GJA1 gene that codes… (More)
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2006
2006
Oculo-dento-digital dysplasia (ODDD) is a rare autosomal dominant congenital disorder mainly affecting the development of the… (More)
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2005
Highly Cited
2005
Oculodentodigital dysplasia (ODDD) is an autosomal dominant disorder characterized by pleiotropic developmental anomalies of the… (More)
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2005
2005
Oculo-dento-digital dysplasia (ODDD, OMIM no. 164210) is a pleiotropic disorder characterized mainly by ocular anomalies, varying… (More)
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2005
2005
Oculodentodigital dysplasia (ODDD) is a rare autosomal dominant pleiotropic disorder, caused by mutations in the Connexin 43 gene… (More)
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2004
2004
Oculodentodigital dysplasia (ODDD) and Hallermann-Streiff syndrome (HSS) share several clinical characteristics. However, while… (More)
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2004
2004
Oculo-dento-digital dysplasia (ODDD) [OMIM 164200] is a rare autosomal dominant pleiotropic disorder comprising ocular… (More)
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