Molecular Basis of Congenital Glaucoma

Zusatztext

A wonderful walk into the world of eye genetics. A 'role model' for all researchers. This piece demonstrates that other known and unknown genes may contribute to Primary Congenital Glaucoma (PCG) pathogenesis. Lack of CYP1B1 gene mutations in some patients stresses the need to identify other responsible candidates. More analysis and screening may be needed and to study Pigmentary Dispersion Syndrome (PDS) genetics.

Autorenportrait

My years of study and indefatigable practice, has prepared me for this role. I have attained skills in teaching, and experience in learning and working independently. I'm an innovative researcher and a University lecturer. I have done my MSc and published several articles in eye care and vision sciences. I'm going to do a PhD in Vision Sciences.

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