P255 – 1787 Optic atrophy plus, a unique phenotype to a known mutation with early onset and rapid progression

Authors :: Dorit Lev
Lubov Blumkin
Esther Leshinsky-Silver
Y Cohen Rappaport
Tally Lerman-Sagie
Source :: European Journal of Paediatric Neurology. 17:S123
Publication Year :: 2013
Publisher :: Elsevier BV, 2013.

Subjects :: Atrophy
Pediatrics, Perinatology and Child Health
Mutation (genetic algorithm)
Cancer research
medicine
Neurology (clinical)
General Medicine
Biology
medicine.disease
Phenotype
Early onset

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