Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Théodora Mayard"'
Autor:
Laurence Pacot, Cyril Burin des Roziers, Ingrid Laurendeau, Audrey Briand-Suleau, Audrey Coustier, Théodora Mayard, Camille Tlemsani, Laurence Faivre, Quentin Thomas, Diana Rodriguez, Sophie Blesson, Hélène Dollfus, Yvon-Gauthier Muller, Béatrice Parfait, Michel Vidaud, Brigitte Gilbert-Dussardier, Catherine Yardin, Benjamin Dauriat, Christian Derancourt, Dominique Vidaud, Eric Pasmant
Publikováno v:
Genes, Vol 10, Iss 9, p 633 (2019)
Neurofibromatosis type 1 (NF1) is an autosomal dominant disease with complete penetrance but high variable expressivity. NF1 is caused by loss-of-function mutations in the NF1 gene, a negative regulator of the RAS-MAPK pathway. The NF1 gene has one o
Externí odkaz:
https://doaj.org/article/ce9a3886345e4722af2f94fbdd2d87b6
Autor:
Cyril Burin des Roziers, Benjamin Dauriat, Michel Vidaud, Laurence Pacot, Hélène Dollfus, Catherine Yardin, Brigitte Gilbert-Dussardier, Camille Tlemsani, Audrey Coustier, Christian Derancourt, Audrey Briand-Suleau, Yvon-Gauthier Muller, Sophie Blesson, Eric Pasmant, Dominique Vidaud, Ingrid Laurendeau, Diana Rodriguez, Quentin Thomas, Laurence Faivre, Béatrice Parfait, Théodora Mayard
Publikováno v:
Genes
Volume 10
Issue 9
Genes, MDPI, 2019, 10 (9), pp.633. ⟨10.3390/genes10090633⟩
Genes, 2019, 10 (9), pp.633. ⟨10.3390/genes10090633⟩
Genes, Vol 10, Iss 9, p 633 (2019)
Volume 10
Issue 9
Genes, MDPI, 2019, 10 (9), pp.633. ⟨10.3390/genes10090633⟩
Genes, 2019, 10 (9), pp.633. ⟨10.3390/genes10090633⟩
Genes, Vol 10, Iss 9, p 633 (2019)
Neurofibromatosis type 1 (NF1) is an autosomal dominant disease with complete penetrance but high variable expressivity. NF1 is caused by loss-of-function mutations in the NF1 gene, a negative regulator of the RAS-MAPK pathway. The NF1 gene has one o
Autor:
Laurence, Pacot, Cyril, Burin des Roziers, Ingrid, Laurendeau, Audrey, Briand-Suleau, Audrey, Coustier, Théodora, Mayard, Camille, Tlemsani, Laurence, Faivre, Quentin, Thomas, Diana, Rodriguez, Sophie, Blesson, Hélène, Dollfus, Yvon-Gauthier, Muller, Béatrice, Parfait, Michel, Vidaud, Brigitte, Gilbert-Dussardier, Catherine, Yardin, Benjamin, Dauriat, Christian, Derancourt, Dominique, Vidaud, Eric, Pasmant
Publikováno v:
Genes
Neurofibromatosis type 1 (NF1) is an autosomal dominant disease with complete penetrance but high variable expressivity. NF1 is caused by loss-of-function mutations in the NF1 gene, a negative regulator of the RAS-MAPK pathway. The NF1 gene has one o