Heterozygosity for an exon 12 splicing mutation and a W234G missense mutation in an American child with chronic tyrosinemia type 1 (Q28288691)

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Heterozygosity for an exon 12 splicing mutation and a W234G missense mutation in an American child with chronic tyrosinemia type 1
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    Heterozygosity for an exon 12 splicing mutation and a W234G missense mutation in an American child with chronic tyrosinemia type 1 (English)
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    S H Hahn
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    D Krasnewich
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    M Brantly
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    E A Kvittingen
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    W A Gahl
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    1995
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    6
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    1
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    66-73
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