Double mutation (A171T and D444H) is a common cause of profound biotinidase deficiency in children ascertained by newborn screening the the United States. Mutations in brief no. 128. Online (Q44859801)
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scientific article published in January 1998
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Double mutation (A171T and D444H) is a common cause of profound biotinidase deficiency in children ascertained by newborn screening the the United States. Mutations in brief no. 128. Online |
scientific article published in January 1998 |
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Double mutation (A171T and D444H) is a common cause of profound biotinidase deficiency in children ascertained by newborn screening the the United States. Mutations in brief no. 128. Online (English)
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K J Norrgard
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R J Pomponio
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K L Swango
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J Hymes
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T Reynolds
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G A Buck
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B Wolf
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1 January 1998
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11
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410
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