Literature DB >> 1301943

A 22-bp deletion in the phenylalanine hydroxylase gene causing phenylketonuria in an Arab family.

S Kleiman1, G Schwartz, S L Woo, Y Shiloh.   

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Year:  1992        PMID: 1301943     DOI: 10.1002/humu.1380010414

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


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  1 in total

1.  Analysis of the phenylalanine hydroxylase gene in the Spanish population: mutation profile and association with intragenic polymorphic markers.

Authors:  B Pérez; L R Desviat; M Ugarte
Journal:  Am J Hum Genet       Date:  1997-01       Impact factor: 11.025

  1 in total

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