domingo, 17 de diciembre de 2017

Orphanet Journal of Rare Diseases | Home page

Orphanet Journal of Rare Diseases | Home page



New Articles For BioMed Central:

Orphanet Journal of Rare Diseases

The following new articles have just been published in Orphanet Journal of Rare Diseases

LETTER TO THE EDITOR

Morphoproteomics and biomedical analytics coincide with clinical outcomes in supporting a constant but variable role for the mTOR pathway in the biology of congenital hyperinsulinism of infancy

Robert E. Brown, Senthil Senniappan, Khalid Hussain and Mary F. McGuire
Orphanet Journal of Rare Diseases 2017, 12:181 | Published on: 16 December 2017

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