logo-large
  • Browse Categories

Publications by authors named "Eneli Haamer"

Claim this Profile
A
Association of unilateral lattice corneal dystrophy on slit lamp and bilateral confocal microscopy features with H572R mutation in the TGFBI gene.
Ricardo De Sousa Peixoto, Stacey Mutch, Jacqueline Eason, Kaie Jaakson, Eneli Haamer

Eye (Lond)· December 2019


Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel mutation and phenotypes in phosphodiesterase 6 deficiency.
Stephen H Tsang, Irena Tsui, Chai Lin Chou, Jana Zernant, Eneli Haamer

Am J Ophthalmol· November 2008


Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Carrier of R14W in carbonic anhydrase IV presents Bothnia dystrophy phenotype caused by two allelic mutations in RLBP1.
Linda Köhn, Marie S I Burstedt, Frida Jonsson, Konstantin Kadzhaev, Eneli Haamer

Invest Ophthalmol Vis Sci· July 2008


Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene.
Lorraine N Clark, Eneli Haamer, Helen Mejia-Santana, Juliette Harris, Suzanne Lesage

Mov Disord· May 2007


Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
© PubHawk
  • About PubHawk
  • Privacy Policy
  • Sitemap
Socials: