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Congenital Disorder Of Glycosylation, Type Im
Known as:
DOLICHOL KINASE DEFICIENCY
, DK1 DEFICIENCY
, CDGIm
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National Institutes of Health
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Related topics
Related topics
7 relations
Autosomal recessive inheritance
Cardiomyopathy, Dilated
DOLK, MET1?
DOLK, TRP304CYS
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Broader (1)
Congenital Disorders of Glycosylation
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
ReportA novel mutation and first report of dilated cardiomyopathy in ALG 6-CDG ( CDG-Ic ) : a case report
M. Al‐Owain
,
Sarar Mohamed
,
N. Kaya
,
Ahmad Zagal
,
G. Matthijs
,
J. Jaeken
2015
Corpus ID: 1019353
Congenital disorders of glycosylation (CDG) are an expanding group of inherited metabolic diseases with multisystem involvement…
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2009
2009
HUBUNGAN KARAKTERISTIK IBU HAMIL DENGAN KEPATUHANDALAM PEMERIKSAAN ANTENATAL CAREDI RB WIDURI SLEMAN YOGYAKARTATAHUN 2009
Nur Hayati
2009
Corpus ID: 181389729
Kematian ibu pada umumnya dapat dicegah bila komplikasi kehamilan dan keadaan resiko tinggi lainnya dapat dideteksi sejak dini…
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