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Going to the first ever Bosch Boonstra Schaaf optic atrophy
BOSCH BOONSTRA SCHAAF OPTIC ATROPHY SYNDROME Semantic Scholar
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Sidelle BOSCH BOONSTRA SCHAAF OPTIC ASTROPHY SYNDROME SWEET
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NR2F1 shapes mitochondria in the mouse brain providing new
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Sidelle BOSCH BOONSTRA SCHAAF OPTIC ASTROPHY SYNDROME SWEET
Bosch Boonstra Schaaf Optic Atrophy Syndrome Hypotonia
NR2F1 Foundation For those with rare NR2F1 gene mutation
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Christian SCHAAF Professor and Chair MD PhD Universit t
Disorder Film Festival Offers Look at Siblings Touched by Rare
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Novel dominant negative NR2F1 frameshift mutation and a phenotypic
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Photos of the patients diagnosed in this study. a Rubinstein
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Today is the 1st BBSOAS International NR2F1 Foundation
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Sidelle BOSCH BOONSTRA SCHAAF OPTIC ASTROPHY SYNDROME SWEET
The expanding clinical phenotype of Bosch Boonstra Schaaf optic
Bosch Boonstra Schaaf Optic Atrophy Syndrome Epilepsy
