Published on IRCCS materno infantile Burlo Garofolo (https://www.burlo.trieste.it)

Home > Printer-friendly > Identification of a New Mutation (L46P) in the Human NOG Gene in an Italian Patient with Symphalangism Syndrome.

Identification of a New Mutation (L46P) in the Human NOG Gene in an Italian Patient with Symphalangism Syndrome. [1]

TitoloIdentification of a New Mutation (L46P) in the Human NOG Gene in an Italian Patient with Symphalangism Syndrome.
Publication TypeJournal Article
AuthorsAthanasakis, E [2], Biarnés, X [3], Bonati, MT [4], Gasparini, P [5], Faletra, F [6]
PubMed ID22855651 [7]
PubMed Central IDPMC3398819
Source URL: https://www.burlo.trieste.it/ricerca/pubblicazioni/identification-new-mutation-l46p-human-nog-gene-italian-patient-symphalangism-syndrome#comment-0

Collegamenti
[1] https://www.burlo.trieste.it/ricerca/pubblicazioni/identification-new-mutation-l46p-human-nog-gene-italian-patient-symphalangism-syndrome
[2] https://www.burlo.trieste.it/ricerca/biblio?f%5Bauthor%5D=705
[3] https://www.burlo.trieste.it/ricerca/biblio?f%5Bauthor%5D=2213
[4] https://www.burlo.trieste.it/ricerca/biblio?f%5Bauthor%5D=2214
[5] https://www.burlo.trieste.it/ricerca/biblio?f%5Bauthor%5D=1341
[6] https://www.burlo.trieste.it/ricerca/biblio?f%5Bauthor%5D=1339
[7] http://www.ncbi.nlm.nih.gov/pubmed/22855651?dopt=Abstract