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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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Bibliographic Details
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.
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
Description
ISSN:09608966
DOI:10.1016/j.nmd.2021.07.006