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Hyperphenylalaninemia, BH4 Deficient (HPABH4)

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Genetic Syndromes
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OMIM: #261640, #233910, #261630, AND #264070

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Correspondence to Andres Morales Corado .

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Corado, A.M. (2023). Hyperphenylalaninemia, BH4 Deficient (HPABH4). In: Rezaei, N. (eds) Genetic Syndromes. Springer, Cham. https://doi.org/10.1007/978-3-319-66816-1_1759-1

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  • DOI: https://doi.org/10.1007/978-3-319-66816-1_1759-1

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  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-319-66816-1

  • Online ISBN: 978-3-319-66816-1

  • eBook Packages: Springer Reference MedicineReference Module Medicine

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