The first case of a complete deficiency of diphosphoglycerate mutase in human erythrocytes.

R Rosa, MO Prehu, Y Beuzard… - The Journal of clinical …, 1978 - Am Soc Clin Investig
An inherited and complete deficiency of diphosphoglycerate mutase was discovered in the
erythrocytes of a 42-yr-old man of French origin whose blood hemoglobin concentration was …

[PDF][PDF] The First Case of a Complete Deficiency of Diphosphoglycerate Mutase in Human Erythrocytes

U MWdicale, HMH Monidor, F Creteil - 1978 - Citeseer
An inherited and complete deficiency of diphosphoglycerate mutase was discovered in the
erythrocytes of a 42-yr-old man of French origin whose blood hemoglobin concentration was …

[PDF][PDF] The First Case of a Complete Deficiency of Diphosphoglycerate Mutase in Human Erythrocytes

U MWdicale, HMH Monidor, F Creteil - 1978 - researchgate.net
An inherited and complete deficiency of diphosphoglycerate mutase was discovered in the
erythrocytes of a 42-yr-old man of French origin whose blood hemoglobin concentration was …

[PDF][PDF] The First Case of a Complete Deficiency of Diphosphoglycerate Mutase in Human Erythrocytes

U MWdicale, HMH Monidor, F Creteil - 1978 - Am Soc Clin Investig
An inherited and complete deficiency of diphosphoglycerate mutase was discovered in the
erythrocytes of a 42-yr-old man of French origin whose blood hemoglobin concentration was …

The first case of a complete deficiency of diphosphoglycerate mutase in human erythrocytes.

R Rosa, MO Prehu, Y Beuzard… - The Journal of Clinical …, 1978 - europepmc.org
An inherited and complete deficiency of diphosphoglycerate mutase was discovered in the
erythrocytes of a 42-yr-old man of French origin whose blood hemoglobin concentration was …

The first case of a complete deficiency of diphosphoglycerate mutase in human erythrocytes

R Rosa, MO Prehu, Y Beuzard… - The Journal of clinical …, 1978 - pubmed.ncbi.nlm.nih.gov
An inherited and complete deficiency of diphosphoglycerate mutase was discovered in the
erythrocytes of a 42-yr-old man of French origin whose blood hemoglobin concentration was …

The first case of a complete deficiency of diphosphoglycerate mutase in human erythrocytes.

R Rosa, MO Prehu, Y Beuzard… - Journal of Clinical …, 1978 - ncbi.nlm.nih.gov
An inherited and complete deficiency of diphosphoglycerate mutase was discovered in the
erythrocytes of a 42-yr-old man of French origin whose blood hemoglobin concentration was …

[引用][C] THE FIRST CASE OF A COMPLETE DEFICIENCY OF DIPHOSPHOGLYCERATE MUTASE IN HUMAN ERYTHROCYTES

R ROSA, P MO, Y BEUZARD, J ROSA - 1978 - pascal-francis.inist.fr
THE FIRST CASE OF A COMPLETE DEFICIENCY OF DIPHOSPHOGLYCERATE MUTASE
IN HUMAN ERYTHROCYTES CNRS Inist Pascal-Francis CNRS Pascal and Francis …