Molecular analysis of maple syrup urine disease in Jordanian families
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文摘

We examined mutations in families with maple syrup urine disease (MSUD).

This is the first report of mutations in Jordanian and Iraqi families with MSUD.

Four different mutations in the BCKDHA gene were identified.

Two others novel missense mutations were found in the DBT gene.

These two mutations may affect the assembly of the intermediate E2 trimer.

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