Deletions within COL11A1 in Type 2 stickler syndrome detected by multiplex ligation-dependent probe amplification (MLPA)

BACKGROUND: COL11A1 is a large complex gene around 250 kb in length and consisting of 68 exons. Pathogenic mutations in the gene can result in Stickler syndrome, Marshall syndrome or Fibrochondrogenesis. Many of the mutations resulting in either Stickler or Marshall syndrome alter splice sites and r...

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Detalles Bibliográficos
Autores principales: Vijzelaar, Raymon, Waller, Sarah, Errami, Abdellatif, Donaldson, Alan, Lourenco, Teresa, Rodrigues, Marcia, McConnell, Vivienne, Fincham, Gregory, Snead, Martin, Richards, Allan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3652776/
https://www.ncbi.nlm.nih.gov/pubmed/23621912
http://dx.doi.org/10.1186/1471-2350-14-48

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3652776/
https://www.ncbi.nlm.nih.gov/pubmed/23621912
http://dx.doi.org/10.1186/1471-2350-14-48

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