Literature DB >> 5442719

Two siblings of hyperphenylalaninemia: suggestion to a genetic variant of phenylketonuria.

K Tada, T Yoshida, K Mochizuki, T Konno, H Nakagawa.   

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Year:  1970        PMID： 5442719     DOI： 10.1620/tjem.100.249

Source DB:  PubMed          Journal:  Tohoku J Exp Med        ISSN： 0040-8727            Impact factor:   1.848


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  3 in total

1.  Mini-symposium: newborn screening for inborn errors of metabolism--clinical effectiveness.

Authors:  Bridget Wilcken
Journal:  J Inherit Metab Dis       Date:  2006 Apr-Jun       Impact factor: 4.982

2.  Tetrahydrobiopterin non-responsiveness in dihydropteridine reductase deficiency is associated with the presence of mutant protein.

Authors:  R G Cotton; I Jennings; G Bracco; A Ponzone; O Guardamagna
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

3.  [Urinary phenylalanine metabolites in hyperphenylalaninemia (author's transl)].

Authors:  P Koepp
Journal:  Klin Wochenschr       Date:  1976-11-01
  3 in total

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