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raf1 (62) 62
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Human Genetics, ISSN 0340-6717, 2/2016, Volume 135, Issue 2, pp. 209 - 222
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 07/2013, Volume 93, Issue 1, pp. 173 - 180
Journal Article
Human Mutation, ISSN 1059-7794, 11/2015, Volume 36, Issue 11, pp. 1080 - 1087
Journal Article
Molecular Syndromology, ISSN 1661-8769, 10/2012, Volume 3, Issue 4, pp. 145 - 157
The RAS/MAPK pathway proteins with germline mutations in their respective genes are associated with some disorders such as Noonan, LEOPARD (LS),... 
Review Article | Gene | RAR/MAPK pathway | BRAF | PTPN11 | Mutation | RAF1 | LEOPARD | MAPK pathway | RAR | Review
Journal Article
Journal of Pediatrics, The, ISSN 0022-3476, 2011, Volume 159, Issue 6, pp. 1029 - 1035
Journal Article
Current Opinion in Genetics & Development, ISSN 0959-437X, 2009, Volume 19, Issue 3, pp. 230 - 236
Journal Article
Journal Article
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 10/2019, Volume 179, Issue 10, pp. 2083 - 2090
Noonan syndrome (NS) is caused by mutations in more than 10 genes, mainly PTPN11 , SOS1 , RAF1 , and RIT1 . Congenital heart defects and cardiomyopathy (CMP)... 
cardiomyopathy | SOS1 | RASopathies | HYPERTROPHIC CARDIOMYOPATHY | GENOTYPE | DISEASE | GENES | GENETICS & HEREDITY | OF-FUNCTION MUTATIONS | RAF1 | Literature reviews | Noonan's syndrome | Mutation | Cardiomyopathy | Morbidity
Journal Article
Journal Article