DOI:
10.1055/s-00000031
Klinische Monatsblätter für Augenheilkunde
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References
Swaroop A, Wang QL, Wu W. et al.
Leber congenital amaurosis caused by a homozygous mutation (R90 W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function.
Hum Mol Genet 1999;
8: 299-305
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