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Identification of a gene disrupted by a microdeletion in a patient with X-linked retinitis pigmentosa (XLRP).
Roepman, R; Bauer, D; Rosenberg, T; van Duijnhoven, G; van de Vosse, E; Platzer, M; Rosenthal, A; Ropers, H H; Cremers, F P; Berger, W.
Affiliation
  • Roepman R; Department of Human Genetics, University Hospital Nijmegen, The Netherlands.
Hum Mol Genet ; 5(6): 827-33, 1996 Jun.
Article in En | MEDLINE | ID: mdl-8776599
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Collection: 01-internacional Database: MEDLINE Main subject: Retinitis Pigmentosa / Gene Deletion Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 1996 Document type: Article Affiliation country: Netherlands Country of publication: United kingdom
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Retinitis Pigmentosa / Gene Deletion Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 1996 Document type: Article Affiliation country: Netherlands Country of publication: United kingdom