rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
Abnormal Newborn Screening in a Healthy Infant of a Mother with Undiagnosed Medium-Chain Acyl-CoA Dehydrogenase Deficiency.
|
25763512 |
2015 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
Medium-chain acyl-CoA dehydrogenase deficiency associated with a novel splice mutation in the ACADM gene missed by newborn screening.
|
26223887 |
2015 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
Child Neurology: medium-chain acyl-coenzyme A dehydrogenase deficiency.
|
26215884 |
2015 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
Selected reaction monitoring as an effective method for reliable quantification of disease-associated proteins in maple syrup urine disease.
|
25333063 |
2014 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
Synthesis framework estimating prevalence of MCADD and sensitivity of newborn screening programme in the absence of direct evidence.
|
24998633 |
2014 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
Pathogenic variants for Mendelian and complex traits in exomes of 6,517 European and African Americans: implications for the return of incidental results.
|
25087612 |
2014 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
Experimental evidence for protein oxidative damage and altered antioxidant defense in patients with medium-chain acyl-CoA dehydrogenase deficiency.
|
24623196 |
2014 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
The domain-specific and temperature-dependent protein misfolding phenotype of variant medium-chain acyl-CoA dehydrogenase.
|
24718418 |
2014 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
Regional differences in the frequency of the c.985A>G ACADM mutation: findings from a meta-regression of genotyping and screening studies.
|
23574375 |
2014 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
Functional studies of 18 heterologously expressed medium-chain acyl-CoA dehydrogenase (MCAD) variants.
|
24966162 |
2014 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
The newborn screen was suggestive for MCAD deficiency, a diagnosis that was confirmed on genetic analysis that showed homozygosity for the disease-associated missense A985G mutation in the ACADM gene.
|
24799540 |
2014 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
Newborn screening for medium-chain acyl-CoA dehydrogenase deficiency: regional experience and high incidence of carnitine deficiency.
|
23842438 |
2013 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
An empirical estimate of carrier frequencies for 400+ causal Mendelian variants: results from an ethnically diverse clinical sample of 23,453 individuals.
|
22975760 |
2013 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
Personalized genomic disease risk of volunteers.
|
24082139 |
2013 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
In vitro and in vivo consequences of variant medium-chain acyl-CoA dehydrogenase genotypes.
|
23509891 |
2013 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
Risk stratification by residual enzyme activity after newborn screening for medium-chain acyl-CoA dehyrogenase deficiency: data from a cohort study.
|
22630369 |
2012 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
Functional effects of different medium-chain acyl-CoA dehydrogenase genotypes and identification of asymptomatic variants.
|
23028790 |
2012 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
Carrier testing for severe childhood recessive diseases by next-generation sequencing.
|
21228398 |
2011 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
Lack of genotype-phenotype correlations and outcome in MCAD deficiency diagnosed by newborn screening in New York State.
|
20036593 |
2010 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
Protein misfolding is the molecular mechanism underlying MCADD identified in newborn screening.
|
19224950 |
2009 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
Dissection of biochemical borderline phenotypes in carriers and genetic variants of medium-chain acyl-CoA dehyrogenase deficiency: implications for newborn screening [corrected].
|
19780764 |
2009 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
Hypoketotic hypoglycemia with myolysis and hypoparathyroidism: an unusual association in medium chain acyl-CoA desydrogenase deficiency (MCADD).
|
20333879 |
2009 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
In mass-screened newborn populations, the 985A>G (K329E) mutation accounts for 54-90% of disease alleles, with homozygotes representing about 47-80% of MCAD deficiency cases.
|
16763904 |
2007 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
The natural history of medium-chain acyl CoA dehydrogenase deficiency in the Netherlands: clinical presentation and outcome.
|
16737882 |
2006 |
rs77931234
|
|
G |
0.900 |
CausalMutation |
CLINVAR |
Population spectrum of ACADM genotypes correlated to biochemical phenotypes in newborn screening for medium-chain acyl-CoA dehydrogenase deficiency.
|
15832312 |
2005 |