Scientists have discovered a new role for a protein that is mutated in Usher syndrome, one of the most common forms of deaf-blindness in humans. The findings may help explain why this mutation causes the most severe form of the condition.
Scientists have discovered a new role for a protein that is mutated in Usher syndrome, one of the most common forms of deaf-blindness in humans. The findings may help explain why this mutation causes the most severe form of the condition.