Publication | Open Access

Spectrum of MEK1 and MEK2 gene mutations in cardio-facio-cutaneous syndrome and genotype–phenotype correlations

Mendelian DisorderCardio-facio-cutaneous SyndromeGenetic DisorderGeneticsGenotype–phenotype CorrelationsPathologyMedical GeneticsDisease Gene IdentificationDermatologyMedicineMek2 Gene MutationsCardiovascular Genetics