<\/figure>\n \n <\/div>\n <\/div>\n \n <\/div>\n \n<\/div>\n","protected":false},"excerpt":{"rendered":"Forschung Das Forschungsprogramm der Carter Foundation Die Mission der Carter Foundation ist es, die Entwicklung von Therapien und Behandlungen f\u00fcr Kinder mit Heredit\u00e4rer Spastischer Paraplegie (HSP) zu erm\u00f6glichen. Derzeit konzentriert sie sich auf die zwei h\u00e4ufigsten Formen von HSP, SPG3A und SPG4, mit Schwerpunkt auf Mutationen mit fr\u00fchem Beginn und oft de-novo-Bedingungen. Das Ziel der […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"ghostkit_customizer_options":"","ghostkit_custom_css":"","ghostkit_custom_js_head":"","ghostkit_custom_js_foot":"","ghostkit_typography":"","footnotes":""},"class_list":["post-150","page","type-page","status-publish","hentry"],"blocksy_meta":{"background":{"background_type":"image","background_pattern":"type-1","background_image":{"attachment_id":154,"x":0,"y":0,"url":"https:\/\/kidswithspg3a.com\/wp-content\/uploads\/2025\/04\/635f4a6c6c5db63aa2f18407_Layer-0-1-613x1024.png"},"gradient":"linear-gradient(135deg,rgba(6,147,227,1) 0%,rgb(155,81,224) 100%)","background_repeat":"repeat","background_size":"cover","background_attachment":"scroll","patternColor":{"default":{"color":"#e5e7ea"}},"overlayColor":{"default":{"color":"CT_CSS_SKIP_RULE"}},"backgroundColor":{"default":{"color":"#ffffff"}}},"styles_descriptor":{"styles":{"desktop":"[data-prefix=\"single_page\"] {background-position:0% 0%;background-size:cover;background-color:#ffffff;background-image:url(https:\/\/kidswithspg3a.com\/wp-content\/uploads\/2025\/04\/635f4a6c6c5db63aa2f18407_Layer-0-1-scaled.png);}","tablet":"","mobile":""},"google_fonts":[],"version":6},"has_hero_section":"disabled"},"_links":{"self":[{"href":"https:\/\/kidswithspg3a.com\/de\/wp-json\/wp\/v2\/pages\/150","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/kidswithspg3a.com\/de\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/kidswithspg3a.com\/de\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/kidswithspg3a.com\/de\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/kidswithspg3a.com\/de\/wp-json\/wp\/v2\/comments?post=150"}],"version-history":[{"count":16,"href":"https:\/\/kidswithspg3a.com\/de\/wp-json\/wp\/v2\/pages\/150\/revisions"}],"predecessor-version":[{"id":213,"href":"https:\/\/kidswithspg3a.com\/de\/wp-json\/wp\/v2\/pages\/150\/revisions\/213"}],"wp:attachment":[{"href":"https:\/\/kidswithspg3a.com\/de\/wp-json\/wp\/v2\/media?parent=150"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}