{"product_id":"hemoglobinopathy-s-von-anelys-garcia-salgado-und-nelson-alvarez-capote","title":"Hemoglobinopathy S","description":"\u003cp\u003eHemoglobinopathy S is an entity that includes all congenital hemolytic anemias in which the gene coding for Hb S is inherited. Worldwide there are an estimated 300 million people recognized as hemoglobin S carriers. There are an estimated 300 million people in the world recognized as carriers of hemoglobin S (Hb S), a condition resulting from the substitution of glutamic acid for valine at position 6 of the ¿-globin gene on the short arm of chromosome 11, which are characterized by the inheritance of a normal hemoglobin A gene from one parent and an abnormal mutated gene from the other parent (AS), unlike homozygous individuals in which both mutated genes are present (SS).\u003c\/p\u003e\u003cdiv class=\"aw-variant-hidden-subtitle-div\" id=\"aw-variant-subtitle-9786207239047\"\u003e\u003ch3\u003eHematology\u003c\/h3\u003e\u003c\/div\u003e","brand":"Autorenwelt Shop","offers":[{"title":"Softcover - 9786207239047","offer_id":48298855891269,"sku":"9786207239047","price":43.9,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0940\/0622\/files\/eaf1c8a8-8b9d-4627-a05e-fa1d57733c9a.jpg?v=1760680815","url":"https:\/\/shop.autorenwelt.de\/products\/hemoglobinopathy-s-von-anelys-garcia-salgado-und-nelson-alvarez-capote","provider":"Autorenwelt Shop","version":"1.0","type":"link"}