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A child with an STK11 mutation and Sotos syndrome-like features: can STK11 mutations produce a Sotos syndrome phenocopy?

In accordance with interrelationships between tumour predisposition and somatic overgrowth, the authors present a boy with a familial serine threonine kinase 11 (STK11) mutation and Sotos syndrome-like features. The authors suggest that, analogous to phosphatase and tensin homolog mutations, STK11 m...

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Hlavní autoři: Baynam, Gareth, Schofield, Lyn, Goldblatt, Jack
Médium: Artigo
Jazyk:Inglês
Vydáno: BMJ Publishing Group 2011
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3185393/
https://ncbi.nlm.nih.gov/pubmed/22679258
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr.07.2011.4445
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