Abstract: The present invention relates to a method for diagnosing or predicting a non syndromic autosomal recessive optic atrophy, or a risk of a non syndromic autosomal recessive optic atrophy.
Type:
Application
Filed:
March 23, 2010
Publication date:
May 3, 2012
Applicant:
INSERM (Institut National de la Sante st de la Recherche Medicale)-