TY - CHAP
T1 - Disorders of glycolysis and the pentose phosphate pathway
AU - Wamelink, Mirjam M. C.
AU - Valayannopoulos, Vassili
AU - Garavaglia, Barbara
PY - 2022/6/24
Y1 - 2022/6/24
N2 - Glycolysis which converts each molecule of glucose to two of pyruvate is the most important source of energy in erythrocytes and in some types of skeletal muscle fibres, therefore inherited diseases of glycolysis are mainly characterized by haemolytic anaemia and/or metabolic myopathy. Ten inborn errors of the glycolytic pathway are known. The pentose phosphate pathway consists of two distinct parts: the first part, an oxidative, non-reversible pathway, produces NADPH, and the second part, a non-oxidative, reversible pathway, produces ribose for nucleotide and nucleic acid synthesis and connects intermediates to glycolysis. Four inborn errors in the pentose phosphate pathway (PPP) are known.
AB - Glycolysis which converts each molecule of glucose to two of pyruvate is the most important source of energy in erythrocytes and in some types of skeletal muscle fibres, therefore inherited diseases of glycolysis are mainly characterized by haemolytic anaemia and/or metabolic myopathy. Ten inborn errors of the glycolytic pathway are known. The pentose phosphate pathway consists of two distinct parts: the first part, an oxidative, non-reversible pathway, produces NADPH, and the second part, a non-oxidative, reversible pathway, produces ribose for nucleotide and nucleic acid synthesis and connects intermediates to glycolysis. Four inborn errors in the pentose phosphate pathway (PPP) are known.
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85158067580&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/37152891
U2 - 10.1007/978-3-662-63123-2_7
DO - 10.1007/978-3-662-63123-2_7
M3 - Chapter
C2 - 37152891
SN - 9783662631225
T3 - Inborn Metabolic Diseases: Diagnosis and Treatment
SP - 209
EP - 223
BT - Inborn Metabolic Diseases: Diagnosis and Treatment
PB - Springer Berlin Heidelberg
ER -