Specific alleles of CLN7/MFSD8, a protein that localizes to photoreceptor synaptic terminals, cause a spectrum of nonsyndromic retinal dystrophy

NIHR BioResource-Rare Diseases Consortium, UK Inherited Retinal Disease Consortium

Research output: Contribution to journal › Article › peer-review

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Medicine and Dentistry

Biochemistry, Genetics and Molecular Biology

Neuroscience