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A novel missense Norrie disease mutation associated with a severe ocular phenotype.
Khan, Arif O; Shamsi, Farrukh A; Al-Saif, Amr; Kambouris, Marios.
Affiliation
  • Khan AO; King Khaled Eye Specialist Hospital, Riyadh 11462, Saudi Arabia.
J Pediatr Ophthalmol Strabismus ; 41(6): 361-3, 2004.
Article in En | MEDLINE | ID: mdl-15609522
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Retinal Diseases / Blindness / Mutation, Missense / Genetic Diseases, X-Linked / Eye Proteins / Nerve Tissue Proteins Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans / Infant / Male Language: En Journal: J Pediatr Ophthalmol Strabismus Year: 2004 Document type: Article Affiliation country: Saudi Arabia Country of publication: United States
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Retinal Diseases / Blindness / Mutation, Missense / Genetic Diseases, X-Linked / Eye Proteins / Nerve Tissue Proteins Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans / Infant / Male Language: En Journal: J Pediatr Ophthalmol Strabismus Year: 2004 Document type: Article Affiliation country: Saudi Arabia Country of publication: United States