Transcriptional Hallmarks of Noonan Syndrome and Noonan-Like Syndrome with Loose Anagen Hair

Noonan syndrome (NS) is among the most common nonchromosomal disorders affecting development and growth. NS is genetically heterogeneous, being caused by germline mutations affecting various genes implicated in the RAS signaling network. This network transduces extracellular signals into intracellul...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Ferrero, Giovanni Battista, Picco, Gabriele, Baldassarre, Giuseppina, Flex, Elisabetta, Isella, Claudio, Cantarella, Daniela, Corá, Davide, Chiesa, Nicoletta, Crescenzio, Nicoletta, Timeus, Fabio, Merla, Giuseppe, Mazzanti, Laura, Zampino, Giuseppe, Rossi, Cesare, Silengo, Margherita, Tartaglia, Marco, Medico, Enzo
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Wiley Subscription Services, Inc., A Wiley Company 2012
Aiheet:
Research Articles
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3332054/
https://ncbi.nlm.nih.gov/pubmed/22253195
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.22026
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