3-MCC

 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1995-2016
02419952016

Papers overview

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Review
2016
Review
2016
INTRODUCTION 3-Methyl crotonyl CoA carboxylase (3MCC) deficiency is an inborn error of leucine metabolism whose detection was… (More)
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2016
2016
Holocarboxylase synthetase deficiency is an autosomal recessive disorder of biotin metabolism resulting in multiple carboxylase… (More)
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2016
2016
We report here a case of maternal 3-methylcrotonyl-coenzyme A carboxylase (3-MCC) deficiency in a Korean woman. Her 2 infants had… (More)
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2013
2013
BACKGROUND A hospital information system (HIS) that integrates screening data and interpretation of the data is routinely… (More)
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2012
2012
INTRODUCTION 3-Methyl CoA carboxylase (3-MCC) deficiency is an inborn error of metabolism in the catabolism of the amino acid… (More)
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2010
2010
We report a positive newborn screen for 3-hydroxyisovalerylcarnitine (C(5)OH) with an absence of 3-methylcrotonyl-coenzyme A… (More)
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Review
2008
Review
2008
3-MCC deficiency is among the most common inborn errors of metabolism identified on expanded newborn screening (1:36,000 births… (More)
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2003
2003
Summary: Since the addition of tandem mass spectrometry (MS/MS) to the North Carolina Newborn Screening Program, 20 infants with… (More)
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1998
1998
The enzyme 3-methylcrotonyl-CoA carboxylase (3-MCC) is involved in leucine degradation. Fifteen cases of isolated 3-MCC deÐciency… (More)
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1995
1995
Genetic deficiency of 3-methylcrotonyl-CoA carboxylase (3-MCC) is a rare inborn error of leucine metabolism producing an organic… (More)
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