{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,14]],"date-time":"2026-02-14T14:10:56Z","timestamp":1771078256081,"version":"3.50.1"},"reference-count":0,"publisher":"Oxford University Press (OUP)","issue":"7","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[1997,7,1]]},"DOI":"10.1093\/hmg\/6.7.1109","type":"journal-article","created":{"date-parts":[[2002,7,26]],"date-time":"2002-07-26T22:20:49Z","timestamp":1027722049000},"page":"1109-1115","source":"Crossref","is-referenced-by-count":55,"title":["Autosomal glycogenosis of liver and muscle due to phosphorylase kinase deficiency is caused by mutations in the phosphorylase kinase beta subunit (PHKB)"],"prefix":"10.1093","volume":"6","author":[{"given":"B","family":"Burwinkel","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","container-title":["Human Molecular Genetics"],"original-title":[],"link":[{"URL":"http:\/\/academic.oup.com\/hmg\/article-pdf\/6\/7\/1109\/1528416\/6-7-1109.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2017,8,23]],"date-time":"2017-08-23T04:50:13Z","timestamp":1503463813000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/hmg\/article-lookup\/doi\/10.1093\/hmg\/6.7.1109"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1997,7,1]]},"references-count":0,"journal-issue":{"issue":"7"},"URL":"https:\/\/doi.org\/10.1093\/hmg\/6.7.1109","relation":{},"ISSN":["1460-2083"],"issn-type":[{"value":"1460-2083","type":"electronic"}],"subject":[],"published":{"date-parts":[[1997,7,1]]}}}