SOS1 is the second most common Noonan gene but plays no major role in cardio‐facio‐cutaneous syndrome
AUTOR(ES)
Zenker, Martin
FONTE
BMJ Group
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2597961Documentos Relacionados
- Cardio‐facio‐cutaneous and Noonan syndromes due to mutations in the RAS/MAPK signalling pathway: genotype–phenotype relationships and overlap with Costello syndrome
- A Mutation in the SOS1 Gene Causes Hereditary Gingival Fibromatosis Type 1
- The Arabidopsis thaliana salt tolerance gene SOS1 encodes a putative Na+/H+ antiporter
- Coocorrência de mutações nos genes PTPN11 e SOS1 na síndrome de Noonan: este achado prediz um fenótipo mais grave?
- Oculo-facio-cardio-dental syndrome in three succeeding generations: genotypic data and phenotypic features