Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Hypoglycemia and SLC22A5[original query] |
---|
Cardiomyopathy and carnitine deficiency. Molecular genetics and metabolism 2008 Jun 94 (2): 162-6. Amat di San Filippo Cristina, Taylor Matthew R G, Mestroni Luisa, Botto Lorenzo D, Longo Nico |
Molecular spectrum of SLC22A5 (OCTN2) gene mutations detected in 143 subjects evaluated for systemic carnitine deficiency. Human mutation 2010 Aug 31 (8): E1632-51. Li Fang-Yuan, El-Hattab Ayman W, Bawle Erawati V, Boles Richard G, Schmitt Eric S, Scaglia Fernando, Wong Lee-J |
Functional and molecular studies in primary carnitine deficiency. Human mutation 2017 8 38 (12): 1684-1699. Frigeni Marta, Balakrishnan Bijina, Yin Xue, Calderon Fernanda R O, Mao Rong, Pasquali Marzia, Longo Nico |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: