| Health / Medical Topics |
EYA1 wt Allele
Human EYA1 wild-type allele is located in the vicinity of 8q13.3 and is approximately 165 kb in length. This allele, which encodes eyes absent homolog 1 protein, may be involved in the development of the eyes, ears, branchial arches and kidney. Mutations of this gene are associated with branchiootorenal dysplasia syndrome, branchiootic syndrome, congenital cataracts and ocular anterior segment anomalies. (NCI Thesaurus)
YOU MAY ALSO LIKE
This gene may play a role in organ development.
Material, such as purulent and nonpurulent fluid, cells, or cellular debris, which has escaped from blood vessels and has been deposited in…
The removal of a previously inserted tube from a hollow organ or passageway, often from the airway.
The use of a series of integrated steps whereby a dry powder is conditioned to form a plasticized mass that is forced…
Issue associated with the unintended of projection of device component materials.
Blood coagulation takes place in 3 essential phases. The first phase is the activation of a prothrombin activator complex. The…
