Somatic uniparental disomy of Chromosome 16p in hemimegalencephaly

Hemimegalencephaly (HME) is a heterogeneous cortical malformation characterized by enlargement of one cerebral hemisphere. Somatic variants in mammalian target of rapamycin (mTOR) regulatory genes have been implicated in some HME cases; however, ∼70% have no identified genetic etiology. Here, we scr...

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Detalles Bibliográficos
Autores principales: Griffin, Nicole G., Cronin, Kenneth D., Walley, Nicole M., Hulette, Christine M., Grant, Gerald A., Mikati, Mohamad A., LaBreche, Heather G., Rehder, Catherine W., Allen, Andrew S., Crino, Peter B., Heinzen, Erin L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2017
Materias:
Research Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593155/
https://www.ncbi.nlm.nih.gov/pubmed/28864461
http://dx.doi.org/10.1101/mcs.a001735

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5593155/
https://www.ncbi.nlm.nih.gov/pubmed/28864461
http://dx.doi.org/10.1101/mcs.a001735

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