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SAMD7 gene

Known as: DKFZp686E1583, SAMD7, sterile alpha motif domain containing 7 
 
National Institutes of Health

Papers overview

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2017
2017
Significance Each retinal rod and cone photoreceptor cell subtype expresses a distinct set of genes including the genes encoding… Expand
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2013
2013
Inherited retinal diseases are mainly caused by mutations in genes that are highly expressed in photoreceptors of the retina. The… Expand
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