Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene.

The HLXB9 homeobox gene was recently identified as a locus for autosomal dominant Currarino syndrome, also known as hereditary sacral agenesis (HSA). This gene specifies a 403-amino acid protein containing a homeodomain preceded by a very highly conserved 82-amino acid domain of unknown function; th...

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Hlavní autoři: Hagan, D M, Ross, A J, Strachan, T, Lynch, S A, Ruiz-Perez, V, Wang, Y M, Scambler, P, Custard, E, Reardon, W, Hassan, S, Nixon, P, Papapetrou, C, Winter, R M, Edwards, Y, Morrison, K, Barrow, M, Cordier-Alex, M P, Correia, P, Galvin-Parton, P A, Gaskill, S, Gaskin, K J, Garcia-Minaur, S, Gereige, R, Hayward, R, Homfray, T
Médium: Artigo
Jazyk:Inglês
Vydáno: 2000
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1378009/
https://ncbi.nlm.nih.gov/pubmed/10749657
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