3-M syndrome: a growth disorder associated with IGF2 silencing

3-M syndrome is an autosomal recessive disorder characterised by pre- and post-natal growth restriction, facial dysmorphism, normal intelligence and radiological features (slender long bones and tall vertebral bodies). It is known to be caused by mutations in the genes encoding cullin 7, obscurin-li...

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Detalles Bibliográficos
Autores principales: Murray, P G, Hanson, D, Coulson, T, Stevens, A, Whatmore, A, Poole, R L, Mackay, D J, Black, G C M, Clayton, P E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioScientifica 2013
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3847915/
https://www.ncbi.nlm.nih.gov/pubmed/24148222
http://dx.doi.org/10.1530/EC-13-0065

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3847915/
https://www.ncbi.nlm.nih.gov/pubmed/24148222
http://dx.doi.org/10.1530/EC-13-0065

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