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[HTML][HTML] Epilepsy and BRAF Mutations: Phenotypes, Natural History and Genotype-Phenotype Correlations

DI Battaglia, ML Gambardella, S Veltri, I Contaldo…�- Genes, 2021 - mdpi.com
Objective: Cardiofaciocutaneous syndrome (CFCS) is a rare developmental disorder caused
by upregulated signaling through the RAS-mitogen-activated protein kinase (MAPK)�…
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Epilepsy and BRAF mutations: Phenotypes, natural history and genotype-phenotype correlations

DI Battaglia, ML Gambardella, S Veltri, I Contaldo…�- GENES, 2021 - publicatt.unicatt.it
Objective: Cardiofaciocutaneous syndrome (CFCS) is a rare developmental disorder caused
by upregulated signaling through the RAS-mitogen-activated protein kinase (MAPK)�…
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[CITATION][C] Epilepsy and BRAF Mutations: Phenotypes, Natural History and Genotype-Phenotype Correlations

DI Battaglia, ML Gambardella, S Veltri, I Contaldo… - 2021 - dspace.unitus.it
Cardiofaciocutaneous syndrome (CFCS) is a rare developmental disorder caused by
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[HTML] nih.gov

[HTML][HTML] Epilepsy and BRAF Mutations: Phenotypes, Natural History and Genotype-Phenotype Correlations

DI Battaglia, ML Gambardella, S Veltri, I Contaldo…�- Genes, 2021 - ncbi.nlm.nih.gov
Objective: Cardiofaciocutaneous syndrome (CFCS) is a rare developmental disorder caused
by upregulated signaling through the RAS-mitogen-activated protein kinase (MAPK)�…
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Epilepsy and BRAF Mutations: Phenotypes, Natural History and Genotype-Phenotype Correlations.

DI Battaglia, ML Gambardella, S Veltri, I Contaldo…�- Genes, 2021 - europepmc.org
Objective: Cardiofaciocutaneous syndrome (CFCS) is a rare developmental disorder caused
by upregulated signaling through the RAS-mitogen-activated protein kinase (MAPK)�…
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Epilepsy and BRAF Mutations: Phenotypes, Natural History and Genotype-Phenotype Correlations

DI Battaglia, ML Gambardella, S Veltri, I Contaldo…�- Genes, 2021 - search.proquest.com
Objective: Cardiofaciocutaneous syndrome (CFCS) is a rare developmental disorder caused
by upregulated signaling through the RAS-mitogen-activated protein kinase (MAPK)�…
Cite

Epilepsy and BRAF Mutations: Phenotypes, Natural History and Genotype-Phenotype Correlations.

DI Battaglia, ML Gambardella, S Veltri, I Contaldo…�- …, 2021 - search.ebscohost.com
Objective: Cardiofaciocutaneous syndrome (CFCS) is a rare developmental disorder caused
by upregulated signaling through the RAS-mitogen-activated protein kinase (MAPK)�…
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[PDF] academia.edu

[PDF][PDF] Epilepsy and BRAF Mutations: Phenotypes

DI Battaglia, ML Gambardella, S Veltri…�- Natural History and�…, 2021 - academia.edu
Objective: Cardiofaciocutaneous syndrome (CFCS) is a rare developmental disorder caused
by upregulated signaling through the RAS-mitogen-activated protein kinase (MAPK)�…
Cite

Epilepsy and BRAF Mutations: Phenotypes, Natural History and Genotype-Phenotype Correlations

DI Battaglia, ML Gambardella, S Veltri, I Contaldo…�- …, 2021 - pubmed.ncbi.nlm.nih.gov
Objective Cardiofaciocutaneous syndrome (CFCS) is a rare developmental disorder caused
by upregulated signaling through the RAS-mitogen-activated protein kinase (MAPK)�…
Cite

Epilepsy and BRAF Mutations: Phenotypes, Natural History and Genotype-Phenotype Correlations

DI Battaglia, ML Gambardella, S Veltri, I Contaldo…�- Genes, 2021 - agris.fao.org
Objective: Cardiofaciocutaneous syndrome (CFCS) is a rare developmental disorder caused
by upregulated signaling through the RAS-mitogen-activated protein kinase (MAPK)�…
Cite