Fourteen new mutations of BCKDHA, BCKDHB and DBT genes associated with maple syrup urine disease (MSUD) in Malaysian population

Maple syrup urine disease (MSUD) is a rare autosomal recessive metabolic disorder. This disorder is usually caused by mutations in any one of the genes; BCKDHA, BCKDHB and DBT, which represent E1α, E1β and E2 subunits of the branched-chain α-keto acid dehydrogenase (BCKDH) complex, respectively. Thi...

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Detalles Bibliográficos
Autores principales: Ali, Ernie Zuraida, Ngu, Lock-Hock
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6140420/
https://www.ncbi.nlm.nih.gov/pubmed/30228974
http://dx.doi.org/10.1016/j.ymgmr.2018.08.006

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6140420/
https://www.ncbi.nlm.nih.gov/pubmed/30228974
http://dx.doi.org/10.1016/j.ymgmr.2018.08.006

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