Case Report: Biotinidas Defficiency and Report of 3 Cases
Biotinidase deficiency is a rare metabolic disease that is transmitted as an autosomal recessive trait. The clinical manifestations of the disease are, lactic acidosis, alopecia, ataxia, spastic paraplegia, seizure and developmental delay. Other clinical features are erythematous rash, hearing and v...
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| Format: | Book |
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University of Social Welfare and Rehabilitation Sciences,
2003-07-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |