{"id":20674,"date":"2023-05-31T12:21:53","date_gmt":"2023-05-31T10:21:53","guid":{"rendered":"https:\/\/www.combibreed.nz\/product\/alpha-mannosidosis-amd\/"},"modified":"2024-03-12T15:18:06","modified_gmt":"2024-03-12T14:18:06","slug":"alpha-mannosidosis-amd","status":"publish","type":"product","link":"https:\/\/www.combibreed.nz\/alpha-mannosidosis-amd\/","title":{"rendered":"Alpha-Mannosidosis – AMD"},"content":{"rendered":"

\u03b1-Mannosidosis is an autosomal recessive disease resulting from the deficiency of lysosomal \u03b1-mannosidase (LAMAN). The mutation is proven to be present on the LAMAN gene, which is a frame shift at codon 583. The frame shift is caused due to a deletion (1748del4).<\/p>\n","protected":false},"excerpt":{"rendered":"