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Cone-Rod Dystrophy 7
Known as:
CORD7
National Institutes of Health
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1 relation
Broader (1)
Retinitis Pigmentosa
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2007
2007
Mutation Associated with an Autosomal Dominant Cone-Rod Dystrophy CORD7 Modifies RIM1-Mediated Modulation of Voltage-Dependent Ca2+ Channels
T. Miki
,
Shigeki Kiyonaka
,
+4 authors
Yasou Mori
Channels
2007
Corpus ID: 12359865
Genetic analyses have revealed an association between the gene encoding the Rab3A‑interacting molecule (RIM1) and the autosomal…
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