Infant with early onset bilateral facial and bulbar weakness: Successful treatment of riboflavin in multiple acyl-CoA dehydrogenase deficiency caused by biallelic nonsense FLAD1 variants.
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| Title: | Infant with early onset bilateral facial and bulbar weakness: Successful treatment of riboflavin in multiple acyl-CoA dehydrogenase deficiency caused by biallelic nonsense FLAD1 variants. |
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| Authors: | Lee, Yun Jeong1 (AUTHOR), Kim, Soo Yeon2,3 (AUTHOR), Kim, Man Jin3 (AUTHOR), Kim, Ae Ryoung4 (AUTHOR), Lee, Jong-Mok5 (AUTHOR), Chae, Jong-Hee1,2,3 (AUTHOR) chaeped1@snu.ac.kr |
| Source: | Neuromuscular Disorders. Nov2021, Vol. 31 Issue 11, p1194-1198. 5p. |
| Database: | Academic Search Ultimate |
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