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Cited by 52Glycosylation and Glycoproteins ResearchImmunodeficiency and Autoimmune DisordersGlycogen Storage Diseases and Myoclonus

The DOI matches its Crossref record; the references it cites are not checked yet.

AN APPARENT HOMOZYGOUS X-LINKED DISORDER WITH CARBOHYDRATE-DEFICIENT SERUM GLYCOPROTEINS

Jaeken, J., Eggermont, E., Stibler, H.·1987·The Lancet
DOI 10.1016/s0140-6736(87)91287-6
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References 1 · Cited by 52

Metadata

Authors
Jaeken, J., Eggermont, E., & Stibler, H.
Affiliations
  • KU Leuven (BE)
  • Karolinska Institutet (SE)
Venue
The Lancet
Publisher
Elsevier BV
Published
1987-12
Volume
330
Issue
8572
Pages
1398
ISSN
  • 0099-5355 (ISSN-L)
  • 0140-6736
DOI
10.1016/s0140-6736(87)91287-6
OpenAlex
W2037415053
Cited by
52
References
1
Citations by year
2020: 2 · 2019: 1 · 2018: 2 · 2017: 1 · 2016: 1 · 2012: 1
FWCI
0.94
Type
journal article
Language
en
Open access
closed
Licence
www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations
  • The Lancet (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Glycosylation and Glycoproteins Research
  • Life Sciences › Immunology and Microbiology › Immunology › Immunodeficiency and Autoimmune Disorders
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Glycogen Storage Diseases and Myoclonus
Keywords
X-linked disorders, hemizygosity, serum glycoproteins, glycosylation defects, X chromosome
MeSH terms
Carbohydrates, Child, Child, Preschool, Diseases in Twins, Female, Glucosyltransferases, Glycoproteins, Homozygote, Humans, Infant, Genetic Linkage, Male, Twins, Monozygotic, X Chromosome, N-Acetylglucosaminyltransferases

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CoChat. (2026). Citation check: AN APPARENT HOMOZYGOUS X-LINKED DISORDER WITH CARBOHYDRATE-DEFICIENT SERUM GLYCOPROTEINS. https://app.cochat.ai/papers/10.1016/s0140-6736(87)91287-6
The paper
Jaeken, J., Eggermont, E., & Stibler, H. (1987). AN APPARENT HOMOZYGOUS X-LINKED DISORDER WITH CARBOHYDRATE-DEFICIENT SERUM GLYCOPROTEINS. The Lancet. https://doi.org/10.1016/s0140-6736(87)91287-6