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A novel nonsense mutation, E150X, in the SOX9 gene underlying campomelic dysplasia

Campomelic dysplasia (CD) is an autosomal dominant skeletal malformation syndrome with features including bowed lower limbs with pretibial skin dimpling, hypoplastic scapulae and pelvic bones, and 11 pairs of ribs. Mutations in the SOX9 gene have been identified to cause CD. The gene encodes a trans...

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Principais autores: Vorasuk Shotelersuk, Somchit Jaruratanasirikul, Thivaratana Sinthuwiwat, Waricha Janjindamai
Formato: Artigo
Idioma:Inglês
Publicado: Sociedade Brasileira de Genética 2006-01-01
Series:Genetics and Molecular Biology
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Acceso en liña:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572006000400007
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