A common ancestral origin of the frequent and widespread 2299delG USH2A mutation. | Am J Hum Genet;69(1): 228-34, 2001 Jul. | MEDLINE

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A common ancestral origin of the frequent and widespread 2299delG USH2A mutation.

Dreyer, B; Tranebjaerg, L; Brox, V; Rosenberg, T; Möller, C; Beneyto, M; Weston, M D; Kimberling, W J; Cremers, C W; Liu, X Z; Nilssen, O.

Affiliation

Dreyer B; Department of Medical Genetics, University Hospital and University of Tromsø, N-9037 Tromsø, Norway. bodreyer@fagmed.uit.no

Am J Hum Genet ; 69(1): 228-34, 2001 Jul.

Article in En | MEDLINE | ID: mdl-11402400

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Retinitis Pigmentosa / Extracellular Matrix Proteins / Sequence Deletion / Founder Effect / Deafness / Gene Frequency Type of study: Prognostic_studies Limits: Humans Language: En Journal: Am J Hum Genet Year: 2001 Document type: Article Affiliation country: Country of publication:

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Retinitis Pigmentosa / Extracellular Matrix Proteins / Sequence Deletion / Founder Effect / Deafness / Gene Frequency Type of study: Prognostic_studies Limits: Humans Language: En Journal: Am J Hum Genet Year: 2001 Document type: Article Affiliation country: Country of publication: