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BIOPKU :: International Database of Patients and Mutations causing BH4-responsive HPA/PKU

This website hosts databases of Pediatric Neurotransmitter Disorders (PND), including the locus-specific database of. Variants and BIOPKU genotypes database. Phanylalanine Hydroxylase Locus-Specific Database. No news at the moment. Jaffe, E. K. (2017). New protein structures provide an updated understanding of phenylketonuria. Mol Genet Metab. Epub ahead of press https:/ www.ncbi.nlm.nih.gov/pubmed/2864553. Https:/ www.ncbi.nlm.nih.gov/pubmed/28174686. Van Spronsen, F. J., et al. (2017). ...Any use of da...

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BIOPKU :: International Database of Patients and Mutations causing BH4-responsive HPA/PKU | biopku.org Reviews

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This website hosts databases of Pediatric Neurotransmitter Disorders (PND), including the locus-specific database of. Variants and BIOPKU genotypes database. Phanylalanine Hydroxylase Locus-Specific Database. No news at the moment. Jaffe, E. K. (2017). New protein structures provide an updated understanding of phenylketonuria. Mol Genet Metab. Epub ahead of press https:/ www.ncbi.nlm.nih.gov/pubmed/2864553. Https:/ www.ncbi.nlm.nih.gov/pubmed/28174686. Van Spronsen, F. J., et al. (2017). ...Any use of da...

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BIOPKU :: International Database of Patients and Mutations causing BH4-responsive HPA/PKU | biopku.org Reviews

https://biopku.org

This website hosts databases of Pediatric Neurotransmitter Disorders (PND), including the locus-specific database of. Variants and BIOPKU genotypes database. Phanylalanine Hydroxylase Locus-Specific Database. No news at the moment. Jaffe, E. K. (2017). New protein structures provide an updated understanding of phenylketonuria. Mol Genet Metab. Epub ahead of press https:/ www.ncbi.nlm.nih.gov/pubmed/2864553. Https:/ www.ncbi.nlm.nih.gov/pubmed/28174686. Van Spronsen, F. J., et al. (2017). ...Any use of da...

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BIOPKU :: International Database of Patients and Mutations causing BH4-responsive HPA/PKU

http://www.biopku.org/home/nblau.asp

Gowland Hopkins Award 2005. AsbjÃ rn FÃ llimng Award 2011. Please complete the form to send a message to Professor Blau. What is the answer:. Senior Consultant in Biochemical Genetics. Division of Inborn Metabolic Diseases. Department of General Pediatrics. Im Neuenheimer Feld 430. Any use of data contained within this web site must receive appropriate acknowledgement and credit, meaning you should cite the URL as follows:. Web site and all contents BioPKU.org 2006 - 2015.

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BIOPKU :: International Database of Patients and Mutations causing BH4-responsive HPA/PKU

http://www.biopku.org/home/biopku.asp

BIOPKUdb : Database of Patients and Genotypes Causing HPA/PKU incl. BH4-Responsive Phenotype. Current number of records:. PKU patients w. BH4 test. As of May 23, 2016). Nenad Blau, Heidelberg, Germany. Wyatt Yue, Oxford, UK. Belen Perez, Madrid, Spain. Division of inborn errors of metabolism. Centre of Molecular Biology and Gene Therapy. Brno, Czech Republic. Department of Molecular Biology, Faculty of Natural Sciences, Comenius University. Web site and all contents BioPKU.org 2006 - 2015.

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This website hosts databases of Pediatric Neurotransmitter Disorders (PND), including the locus-specific database of. Variants and BIOPKU genotypes database. Phanylalanine Hydroxylase Locus-Specific Database. No news at the moment. Jaffe, E. K. (2017). New protein structures provide an updated understanding of phenylketonuria. Mol Genet Metab. Epub ahead of press https:/ www.ncbi.nlm.nih.gov/pubmed/2864553. Https:/ www.ncbi.nlm.nih.gov/pubmed/28174686. Van Spronsen, F. J., et al. (2017). ...Any use of da...

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