On the nonaggregation of normal adult hemoglobin and the aggregation of sickle cell hemoglobin
N Galamba - The Journal of Physical Chemistry B, 2019 - ACS Publications
Sickle cell disease is a genetic disorder associated with a single mutation (Glu-β6→ Val-β6)
in the β chains of hemoglobin, causing the polymerization of deoxygenated sickle cell …
in the β chains of hemoglobin, causing the polymerization of deoxygenated sickle cell …
On the Nonaggregation of Normal Adult Hemoglobin and the Aggregation of Sickle Cell Hemoglobin
N Galamba - The journal of physical chemistry. B, 2019 - pubmed.ncbi.nlm.nih.gov
Sickle cell disease is a genetic disorder associated with a single mutation (Glu-β6→ Val-β6)
in the β chains of hemoglobin, causing the polymerization of deoxygenated sickle cell …
in the β chains of hemoglobin, causing the polymerization of deoxygenated sickle cell …
On the Nonaggregation of Normal Adult Hemoglobin and the Aggregation of Sickle Cell Hemoglobin.
N Galamba - The Journal of Physical chemistry. B, 2019 - europepmc.org
Sickle cell disease is a genetic disorder associated with a single mutation (Glu-β6→ Val-β6)
in the β chains of hemoglobin, causing the polymerization of deoxygenated sickle cell …
in the β chains of hemoglobin, causing the polymerization of deoxygenated sickle cell …