View Crispr Cas9 Sickle Cell Anemia Pics. Hbb gene encodes a protein called beta hemoglobin, which is a subunit of a larger protein called hemoglobin. The most common type is known as sickle cell anaemia (sca).

Sickle cell disease (scd) is an inherited monogenic disorder resulting in serious mortality and morbidity worldwide.
Hbb gene encodes a protein called beta hemoglobin, which is a subunit of a larger protein called hemoglobin. Recent discovery of crispr/cas9 has not only revolutionized genome engineering but has also anemia, sickle cell / therapy*. Another genetic disease sickle cell anemia affects around 300,000 neonates globally per year 80. Sickle cell disease (scd) is an inherited monogenic disorder resulting in serious mortality and morbidity worldwide.
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