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Congenital Disorder Of Glycosylation, Type Im

Known as: DOLICHOL KINASE DEFICIENCY, DK1 DEFICIENCY, CDGIm 
National Institutes of Health

Related topics

Related topics

7 relations
Autosomal recessive inheritanceCardiomyopathy, DilatedDOLK, MET1?DOLK, TRP304CYS

Broader (1)

Congenital Disorders of Glycosylation

Papers overview

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Review
2018
Review
2018
Ten years of PAMELA in space
The PAMELA cosmic-ray detector was launched on June 15th 2006 on board the Russian Resurs-DK1 satellite, and during ten years of… 
2015
2015
Boson field mixing in Rindler spacetime
We study the mixing of two complex boson fields with different masses in Rindler spacetime. We find that the Bogoliubov… 
2015
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… 
2009
2009
HUBUNGAN KARAKTERISTIK IBU HAMIL DENGAN KEPATUHANDALAM PEMERIKSAAN ANTENATAL CAREDI RB WIDURI SLEMAN YOGYAKARTATAHUN 2009
Kematian ibu pada umumnya dapat dicegah bila komplikasi kehamilan dan keadaan resiko tinggi lainnya dapat dideteksi sejak dini… 
2002
2002
Comments to Coleman's paper "There are no Goldstone Bosons in Two Dimensions"
We analyse Coleman’s theorem asserting the absence Goldstone bosons and spontaneously broken continuous symmetry in the quantum… 
Highly Cited
2000
Highly Cited
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… 
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