18752264Manzini MC, Gleason D, Chang BS, Hill RS, Barry BJ, Partlow JN, Poduri A, Currier S, Galvin-Parton P, Shapiro LR, Schmidt K, Davis JG, Basel-Vanagaite L, Seidahmed MZ, Salih MA, Dobyns WB, Walsh CAHuman mutationAbnormalities, Multiple; Membrane Proteins; MutationChild; Cobblestone Lissencephaly; DNA Mutational Analysis; Eye Abnormalities; Female; Genome, Human; Genotype; Humans; Male; Middle East; Muscular Dystrophies; Pedigree; Phenotype; SyndromeEthnically diverse causes of Walker-Warburg syndrome (WWS): FCMD mutations are a more common cause of WWS outside of the Middle East. Hum Mutat. 2008 Nov; 29(11):E231-41.Hum Mutat2008-11-01T00:00:002008Ethnically diverse causes of Walker-Warburg syndrome (WWS): FCMD mutations are a more common cause of WWS outside of the Middle East.prns:fullNamefull nameprns:hasAuthorListauthor listprns:hasNetworkhas networkprns:hasPublicationVenuepublished inprns:hasSubjectAreaMajorTopicListhas major subject area listprns:hasSubjectAreaMinorTopicListhas minor subject area listprns:informationResourceReferenceinformation resource referenceprns:isPrimaryPositionis primary positionprns:latitudelatitudeprns:longitudelongitudeprns:maxWeightmaximum weightprns:medlineTAjournal title abbreviationprns:meshDescriptorUIMeSH DescriptorUIprns:meshSemanticGroupNameMeSH semantic group nameprns:minWeightminimum weightprns:numberOfAuthorsnumber of authorsprns:numberOfConnectionsnumber of connectionsprns:numberOfPublicationsnumber of publicationsprns:personIdPerson IDprns:personInPrimaryPositionperson in primary positionprns:positionInDepartmentposition in departmentprns:predicateNodepredicate nodeprns:publicationDatepublication dateprns:sortOrdersort orderprns:uniquenessWeightuniqueness weightprns:yearyearAcademic ArticleArticleDocumentbibo:pmidPubMed Identifiervivo:authorRankauthor rank in publicationAuthorshipDepartmentvivo:hasSubjectAreahas subject areavivo:hrJobTitleHR job titleInformation Resourcevivo:informationResourceInAuthorshipauthorsvivo:linkedAuthorlinked authorvivo:linkedInformationResourcelinked information resourcePositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titlerdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPersonD000015Disorders842320.867856Abnormalities, MultipleD002648Living Beings93969130.440068ChildD004252Procedures2265260.864607DNA Mutational AnalysisD005124Disorders14410.973637Eye AbnormalitiesD008565Chemicals & Drugs37111940.607165Membrane ProteinsD008877Geographic Areas15170.995702Middle EastD009154Physiology70239520.442682MutationD010375Concepts & Ideas1929660.83743PedigreeD005260Physiology1992444050.191184FemaleD006801Living Beings2262862810.130064HumansD013577Disorders2074460.911443SyndromeWilliamDobynsWilliam B. Dobyns0.000000000000000.000000000000002964Dobyns, WilliamPROFESSOR D008297Physiology1931408600.201635MaleD009136Disorders20540.968877Muscular DystrophiesD054222Disorders110.999893Cobblestone LissencephalyD015894Genes & Molecular Sequences1837560.68676Genome, HumanD005838Physiology41118500.686761GenotypeD010641Physiology64723750.61589PhenotypeHuman GeneticsUniversity of Chicagotrue1PROFESSOR PROFESSOR Authorship 75123160.08593630.08593631authors10.2517has subject area