Gerard Schwartz

Gerard Schwartz

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Gerard Schwartz

Gerard Schwartz

Publications by authors named "Gerard Schwartz"

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Man made disease: clinical manifestations of low phenylalanine levels in an inadequately treated phenylketonuria patient and mouse study.

Mol Genet Metab 2013 12;110 Suppl:S66-70. Epub 2013 Oct 12.

Metabolic Disease Unit, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel-Hashomer, Israel.

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https://linkinghub.elsevier.com/retrieve/pii/S10967192130033
Publisher Site
http://dx.doi.org/10.1016/j.ymgme.2013.10.006DOI Listing
July 2014

Genotype-phenotype correlations analysis of mutations in the phenylalanine hydroxylase (PAH) gene.

J Hum Genet 2008 26;53(5):407-18. Epub 2008 Feb 26.

MIGAL, Galilee Technology Center, Human Molecular Genetics and Pharmacogenetics Laboratory, Kiryat Shmona, Israel.

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http://dx.doi.org/10.1007/s10038-008-0264-4DOI Listing
July 2008