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Congenital Disorder Of Glycosylation, Type Im

Known as: Dolichol Kinase Deficiency, DK1 DEFICIENCY, CDGIm 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1992-2015
0119922015

Related topics

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7 relations
Autosomal recessive inheritanceCardiomyopathy, DilatedDOLK, MET1?DOLK, TRP304CYS
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Broader (1)

Congenital Disorders of Glycosylation

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
Congenital Disorder Of Glycosylation, Type Im
Autosomal recessive inheritance
Cardiomyopathy, Dilated
Ichthyoses
Congenital Disorders of Glycosylation
Failure to Thrive

Papers overview

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Review
2015
Review
2015
ReportA novel mutation and first report of dilated cardiomyopathy in ALG 6-CDG ( CDG-Ic ) : a case report
Congenital disorders of glycosylation (CDG) are an expanding group of inherited metabolic diseases with multisystem involvement… (More)
  • figure 1
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2000
2000
Middle Stone Age human fossils from Die Kelders Cave 1, Western Cape Province, South Africa.
Die Kelders Cave 1 (DK1) preserves a thick series of Middle Stone Age (MSA) horizons that date to a fairly short temporal… (More)
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  • table 1
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1992
1992
Some Quantum Analogues of Solvable Lie Groups
Introduction. In the papers [DK1-2],[DKP1-2] the quantized enveloping algebras introduced by Drin-feld and Jimbo have been… (More)
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