Different clinical manifestations of hyperphenylalaninemia in three siblings with identical phenylalanine hydroxylase genes.

Ítems similars

• DNA haplotype analyses of patients with hyperphenylalaninemia.
  per: Di Silvestre, D, et al.
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  per: Kayaalp, E, et al.
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• RFLPs at the PAH (phenylalanine hydroxylase) gene in the Japanese population
  per: Araki, Kiyoshi, et al.
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• Silent mutations in the phenylalanine hydroxylase gene as an aid to the diagnosis of phenylketonuria.
  per: Kalaydjieva, L, et al.
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• Phenylketonuria in U.S. blacks: molecular analysis of the phenylalanine hydroxylase gene.
  per: Hofman, K J, et al.
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