Publication | Closed Access
Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation
31
Citations
47
References
2002
Year
Autosomal Cone-rod DystrophyDevelopmental BiologyMendelian DisorderGenetic DisorderCraniofacial DevelopmentNovel Crx MutationDegenerative DiseasePhenotypic FeaturesNeuropathologyMedicineOrthopaedic Surgery
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