Case Report: A Case of Gait Disorder Due to Combined Methylmalonic Aciduria and Homocystinuria
This disorder is too rare that about 100 patients have been reported in the world. In this condition a liver enzyme (methylmalonyl CoA mutase) which should carry out one of many thousands of chemical processes that turn protein into energy or body tissues is defective. Clinical presentation of this...
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University of Social Welfare and Rehabilitation Sciences,
2000-10-01T00:00:00Z.
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Connect to this object online.3rd Floor Main Library
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A1234.567 |
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