- Tytuł:
- Whole-Exome Sequencing Identifies LRIT3 Mutations as a Cause of Autosomal-Recessive Complete Congenital Stationary Night Blindness
- Autorzy:
- Temat:
-
NIGHT blindness
GENETIC mutation
VISUAL acuity
LEUCINE
IMMUNOGLOBULINS
MEMBRANE proteins
RETINAL diseases - Źródło:
- American Journal of Human Genetics. Jan2013, Vol. 92 Issue 1, p67-75. 9p.
Czasopismo naukowe