Literature DB >> 4169602

A third allele at the phenylalanine-hydroxylase locus in mild phenylketonuria (hyperphenylalaninaemia).

L I Woolf, B L Goodwin, W I Cranston, D N Wade, F Woolf, F P Hudson, M S McBean.   

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Year:  1968        PMID： 4169602     DOI： 10.1016/s0140-6736(68)92722-0

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  8 in total

Review 1.  Phenylketonuria: a review.

Authors:  J S Yu
Journal:  Postgrad Med J       Date:  1970-07       Impact factor: 2.401

2.  Iherited abnormalities affecting the nervous system: genetic and psychiatric aspects.

Authors:  J Stern; V Cowie
Journal:  Biochem J       Date:  1969-02       Impact factor: 3.857

3.  Metabolism of phenylalanine in mice homozygous for the gene 'dilute lethal'.

Authors:  L I Woolf; A Jakubovic; F Woolf; P Bory
Journal:  Biochem J       Date:  1970-10       Impact factor: 3.857

Review 4.  Diseases of phenylalanine metabolism.

Authors:  C E Parker
Journal:  West J Med       Date:  1979-10

5.  Compound heterozygosity in nonphenylketonuria hyperphenylalanemia: the contribution of mutations for classical phenylketonuria.

Authors:  S Avigad; S Kleiman; M Weinstein; B E Cohen; G Schwartz; S L Woo; Y Shiloh
Journal:  Am J Hum Genet       Date:  1991-08       Impact factor: 11.025

6.  Phenylketonuria and its variants: observations on intellectual functioning.

Authors:  C Netley; W B Hanley; H L Rudner
Journal:  Can Med Assoc J       Date:  1984-10-01       Impact factor: 8.262

7.  Incidence of phenylketonuria (PKU) in Iran.

Authors:  D D Farhud; M Kabiri
Journal:  Indian J Pediatr       Date:  1982 Sep-Oct       Impact factor: 1.967

8.  Genetics and biochemistry of the phenylketonuria-present state.

Authors:  K Bartholomé
Journal:  Hum Genet       Date:  1979-10-02       Impact factor: 4.132
  8 in total

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