Severe DengueSeverity of Illness IndexMutationPedigreePhenotypeLeber Congenital AmaurosisHomozygotePelizaeus-Merzbacher DiseaseMutation, MissenseHypophosphatasiaConsanguinityHyperemesis GravidarumDengue VirusDengueDNA Mutational AnalysisInfant, NewbornOsteogenesis ImperfectaAdrenal Hyperplasia, CongenitalFaciesDisease Models, AnimalHypospadiasalpha-ThalassemiaTuberculosis, MeningealHeterozygoteFrameshift MutationSyndromeMucopolysaccharidosis IGenes, RecessiveGenotypeSteroid 21-HydroxylaseIduronidaseExonsLeptospirosisAcne VulgarisPoint MutationSpinal Muscular Atrophies of ChildhoodMolecular Sequence DataHaplotypesMalaria, CerebralOsteochondrodysplasiasCodon, NonsensePolymerase Chain ReactionAge of OnsetFatal OutcomeGenetic Predisposition to DiseaseAIDS Dementia ComplexEye ProteinsCase-Control StudiesAllelesBase SequenceRetinitis PigmentosaMuscular DystrophiesMuscular Atrophy, SpinalPregnancyAbnormalities, MultipleBlindnessRetrospective StudiesRespiratory Distress Syndrome, AdultAcute Lung InjuryAmino Acid SequencePlasmodium falciparumBrazilFamily HealthRisk FactorsChronic DiseaseAcute DiseaseIntellectual DisabilityGenes, DominantTreatment OutcomeIndiaBiological MarkersSequence Analysis, DNADisease ProgressionPancreatitisMice, Inbred C57BLPre-EclampsiaItalyTime FactorsProspective StudiesSkinMice, KnockoutAmino Acid SubstitutionPrevalencePrognosisSequence DeletionEnzyme-Linked Immunosorbent AssayBiopsyPolymorphism, Single NucleotideReverse Transcriptase Polymerase Chain ReactionCells, CulturedGenetic LinkageCohort StudiesBrainMice, TransgenicErythrocytesPolymorphism, GeneticMice, Mutant StrainsFollow-Up StudiesGene DeletionDNA Primers