Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Glycogen Storage Disease and AGL[original query] |
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Molecular genetic basis and prevalence of glycogen storage disease type IIIA in the Faroe Islands. European journal of human genetics : EJHG 2001 May 9 (5): 388-91. Santer R, Kinner M, Steuerwald U, Kjaergaard S, Skovby F, Simonsen H, Shaiu W L, Chen Y T, Schneppenheim R, Schaub |
Spectrum of AGL mutations in Chinese patients with glycogen storage disease type III: identification of 31 novel mutations. Journal of human genetics 2016 Mar . Lu Chaoxia, Qiu Zhengqing, Sun Miao, Wang Wei, Wei Min, Zhang X |
Intron retention is among six unreported AGL mutations identified in Malaysian GSD III patients. Genes & genomics 2019 4 41 (8): 885-893. Abdullah Ili Syazwana, Teh Ser-Huy, Khaidizar Fiqri Dizar, Ngu Lock-Hock, Keng Wee-Teik, Yap Sufin, Mohamed Zulqarna |
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