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dc.contributor.authorTOPALOGLU, HALUK
dc.date.accessioned2019-12-10T10:36:36Z
dc.date.available2019-12-10T10:36:36Z
dc.date.issued2013
dc.identifier.issn1128-2460
dc.identifier.urihttps://doi.org/
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4006280/
dc.identifier.urihttp://hdl.handle.net/11655/13958
dc.description.abstractThe Mediterranean countries are distinguished with their peculiar genetic pool and diversities. Recessive diseases often present with their own founder mutations. In some instances this is shared with neighboring populations. Dominant disorders in the area are increasingly recognized as health care providing systems and technology improve. Among muscular dystrophies Duchenne and Becker types constitute the major fraction in almost all societies. This is followed by various forms of limb-girdle muscular dystrophy. Congenital dystrophies and other related rare types are a matter of recognition. The identification and registry of facio-scapulo-humeral and myotonic dystrophies vary in different states.
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleEpidemiology Of Muscular Dystrophies In The Mediterranean Area
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalActa Myologica
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları
dc.identifier.volume32
dc.identifier.issue3
dc.identifier.startpage138
dc.identifier.endpage141
dc.description.indexPubMed


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