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Ornithine Transcarbamylase Deficiency Website. Welcome to the Ornithine Transcarbamylase website. Ornithine transcarbamylase (OTC) is an enzyme of the. Ornithine transcarbamylase deficiency is an inborn error of metabolism usually caused by mutations in the OTC gene. Ornithine transcarbamylase deficiency affects approximately 1:16000 children, and accounts for nearly half of all inherited urea cycle disorders. Shown below is a schematic of a cell with the various enzymes of the urea cycle highlighted.

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Ornithine Transcarbamylase Deficiency Website. Welcome to the Ornithine Transcarbamylase website. Ornithine transcarbamylase (OTC) is an enzyme of the. Ornithine transcarbamylase deficiency is an inborn error of metabolism usually caused by mutations in the OTC gene. Ornithine transcarbamylase deficiency affects approximately 1:16000 children, and accounts for nearly half of all inherited urea cycle disorders. Shown below is a schematic of a cell with the various enzymes of the urea cycle highlighted.
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Ornithine Transcarbamylase Deficiency Website. Welcome to the Ornithine Transcarbamylase website. Ornithine transcarbamylase (OTC) is an enzyme of the. Ornithine transcarbamylase deficiency is an inborn error of metabolism usually caused by mutations in the OTC gene. Ornithine transcarbamylase deficiency affects approximately 1:16000 children, and accounts for nearly half of all inherited urea cycle disorders. Shown below is a schematic of a cell with the various enzymes of the urea cycle highlighted.

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Glossary

http://ureacycle.cnmcresearch.org/otc/page26/page26.html

Ornithine Transcarbamylase Deficiency Website. 2007 Children's National Medical Center.

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Home

http://ureacycle.cnmcresearch.org/otc/index.html

Ornithine Transcarbamylase Deficiency Website. Welcome to the Ornithine Transcarbamylase website. Ornithine transcarbamylase (OTC) is an enzyme of the. Ornithine transcarbamylase deficiency is an inborn error of metabolism usually caused by mutations in the OTC gene. Ornithine transcarbamylase deficiency affects approximately 1:16000 children, and accounts for nearly half of all inherited urea cycle disorders. Shown below is a schematic of a cell highlighting the various enzymes of the urea cycle.

3

Other Research

http://ureacycle.cnmcresearch.org/otc/page2/page2.html

Ornithine Transcarbamylase Deficiency Website. Some of the other projects that we are studying in the lab. 2007 Children's National Medical Center.

4

Links

http://ureacycle.cnmcresearch.org/otc/page14/page14.html

Ornithine Transcarbamylase Deficiency Website. Wikipedia Ornithine transcarbamylase deficiency. Online Mendelian Inheritance in Man. NIH NLM Genetics Home Reference. National Organization for Rare Disorders. Urea Cycle Disorders Consortium. National Urea Cycle Disorders Foundation. 2007 Children's National Medical Center.

5

Submit New Mutations

http://ureacycle.cnmcresearch.org/otc/page16/page16.html

Ornithine Transcarbamylase Deficiency Website. We are currently testing an online submission and validation system for new mutations. Thank you for your patience. 2007 Children's National Medical Center.

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Ornithine Transcarbamylase Deficiency Website. Welcome to the Ornithine Transcarbamylase website. Ornithine transcarbamylase (OTC) is an enzyme of the. Ornithine transcarbamylase deficiency is an inborn error of metabolism usually caused by mutations in the OTC gene. Ornithine transcarbamylase deficiency affects approximately 1:16000 children, and accounts for nearly half of all inherited urea cycle disorders. Shown below is a schematic of a cell with the various enzymes of the urea cycle highlighted.

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