The genetic mechanism of hereditary human hair diseases, such as alopecia and thinning hair, has drawn much attention in human genetics research, yet many questions around this mechanism persist. A recent animal study in The FASEB Journal revealed that a mutation in the gene that encodes a protein called MAP2 (for “microtubule-associated protein 2”) may be an essential component of the hairless phenotype.
from http://besthealthnews.com/2019/11/animal-study-finds-link-between-map2-mutation-and-hereditary-hair-diseases/?utm_source=rss&utm_medium=rss&utm_campaign=animal-study-finds-link-between-map2-mutation-and-hereditary-hair-diseases
from
https://healthnews010.tumblr.com/post/189223832383
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