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2021
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Refining Genotypes and Phenotypes in
KCNA2
-Related Neurological Disorders.
Not available
S-EPMC7999221
|
biostudies-literature
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Heterozygous truncating variants in SUFU cause congenital ocular motor apraxia.
Not available
S-EPMC7862056
|
biostudies-literature
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