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HEREDITARY HEMOLYTIC DISEASE SECONDARY TO GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY: REPORT OF THREE CASES WITH SPECIAL EMPHASIS ON ATP METABOLISM.
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- Author(s): MOHLER DN; CROCKETT CL Jr
- Source:
Blood [Blood] 1964 Apr; Vol. 23, pp. 427-44.
- Publication Type:
Journal Article
- Language:
English
- Additional Information
- Source:
Publisher: Elsevier Country of Publication: United States NLM ID: 7603509 Publication Model: Print Cited Medium: Print ISSN: 0006-4971 (Print) Linking ISSN: 00064971 NLM ISO Abbreviation: Blood Subsets: OLDMEDLINE
- Publication Information:
Publication: 2021- : [New York] : Elsevier
Original Publication: New York, Grune & Stratton [etc.]
- Subject Terms:
- Contributed Indexing:
Keywords: ADENOSINE TRIPHOSPHATE*; ADOLESCENCE*; ANEMIA, HEMOLYTIC*; CHROMIUM ISOTOPES*; ERYTHROCYTES*; GENETICS, HUMAN*; GLUCOSEPHOSPHATE DEHY- DROGENASE DEFICIENCY*; GLUTATHIONE*; METHEMOGLOBIN*; NAD*; NADP*; PYRUVATES*
- Accession Number:
0 (Chromium Isotopes)
0 (Glucosephosphates)
0 (Pyruvates)
0U46U6E8UK (NAD)
53-59-8 (NADP)
8L70Q75FXE (Adenosine Triphosphate)
9008-37-1 (Methemoglobin)
GAN16C9B8O (Glutathione)
- Publication Date:
Date Created: 19640401 Date Completed: 19961201 Latest Revision: 20181201
- Publication Date:
20250114
- Accession Number:
14138235
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