Literature DB >> 8750617

Phenylketonuria mutations in southern Chinese detected by denaturing gradient gel electrophoresis in exon 7 of PAH gene.

X F Gu1, M Zhang, R G Chen.   

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Year:  1995        PMID： 8750617     DOI： 10.1007/bf02436769

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  4 in total

1.  Computational simulation of DNA melting and its application to denaturing gradient gel electrophoresis.

Authors:  L S Lerman; K Silverstein
Journal:  Methods Enzymol       Date:  1987       Impact factor: 1.600

2.  Twenty-one cases of phenylketonuria out of 358,767 newborns in Shanghai, China.

Authors:  R G Chen; X S Pan; D L Qian; H Guo
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

3.  Detection and localization of single base changes by denaturing gradient gel electrophoresis.

Authors:  R M Myers; T Maniatis; L S Lerman
Journal:  Methods Enzymol       Date:  1987       Impact factor: 1.600

Review 4.  Molecular basis of phenylketonuria and related hyperphenylalaninemias: mutations and polymorphisms in the human phenylalanine hydroxylase gene.

Authors:  R C Eisensmith; S L Woo
Journal:  Hum Mutat       Date:  1992       Impact factor: 4.878
  4 in total
  1 in total

1.  Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population.

Authors:  Tina Shirzadeh; Amir Hossein Saeidian; Hamideh Bagherian; Shadab Salehpour; Aria Setoodeh; Mohammad Reza Alaei; Leila Youssefian; Ashraf Samavat; Andrew Touati; Mohammad-Sadegh Fallah; Hassan Vahidnezhad; Morteza Karimipoor; Sarah Azadmehr; Marzieh Raeisi; Ameneh Bandehi Sarhadi; Fatemeh Zafarghandi Motlagh; Mojdeh Jamali; Zahra Zeinali; Maryam Abiri; Sirous Zeinali
Journal:  J Inherit Metab Dis       Date:  2018-08-29       Impact factor: 4.982
  1 in total

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