A 3-base pair insertional mutation in the choroideremia gene.

Nesslinger, N; Horrocks, S; Ray, P N; Strasberg, P; MacDonald, I M

Nesslinger, N; Horrocks, S; Ray, P N; Strasberg, P; MacDonald, I M.

Affiliation

Nesslinger N; Ocular Genetics Laboratory, Department of Ophthalmology, University of Alberta, Edmonton, Canada.

Hum Mutat ; Suppl 1: S38-9, 1998.

Article in En | MEDLINE | ID: mdl-9452034

Subject(s)

Choroideremia/genetics; Amino Acid Sequence; Base Sequence; Codon, Terminator/genetics; DNA/chemistry; DNA/genetics; DNA Mutational Analysis; Exons/genetics; Family Health; Female; Humans; Male; Mutagenesis, Insertional; Mutation; Polymorphism, Single-Stranded Conformational

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Collection: 01-internacional Database: MEDLINE Main subject: Choroideremia Limits: Female / Humans / Male Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 1998 Document type: Article Affiliation country: Canada Country of publication: United States

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