Publication | Closed Access
X‐linked retinoschisis in a female with a heterozygous <i>RS1</i> missense mutation
19
Citations
10
References
2007
Year
Mendelian DisorderOphthalmologyGenetic DisorderGeneticsCraniofacial DevelopmentGenetic MechanismMolecular GeneticsMedical GeneticsChromosomal RearrangementMedicine
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