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PMID: 5862690 Published · ppublish ger Case Reports Journal Article

[Hexokinase deficiency in blood cells in a group of kin with familial panmyelopathy (Fanconi type)].

Hexokinasemangel in Blutzellen bei einer Sippe mit familiärer Panmyelopathie (Typ Fanconi)

Klinische Wochenschrift ·Vol. 43 ·No. 16 ·1965-08-15 ·Pages 870-5

Löhr GW, Waller HD, Anschütz F, Knopp A

Abstract

暂无摘要

MeSH Terms
Adenosine Triphosphate/metabolism Adolescent Adult Blood Cells/metabolism Blood Platelets Erythrocyte Count Fanconi Syndrome/genetics Glutathione/metabolism Glycolysis Hexokinase/metabolism Humans Leukocyte Count Male Pentosephosphates/metabolism Phosphates/metabolism
Chemicals
Pentosephosphates Phosphates Adenosine Triphosphate Hexokinase Glutathione
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Löhr G W
Waller H D
Anschütz F
Knopp A
References (16)
16 references, click to expand
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Article Info
Journal
Klinische Wochenschrift
Abbr.
Klin Wochenschr
ISSN
0023-2173
DOI
10.1007/BF01711251
Published
1965-08-15
Pages
870-5
Language
ger
Region
Germany
NLM ID
2985205R
Subset
IM
External Links
PubMed source DOI: 10.1007/BF01711251
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