Screening for mutations in exon 4 of the LDL receptor gene: identification of a new deletion mutation. | J Med Genet;32(5): 379-82, 1995 May. | MEDLINE

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Screening for mutations in exon 4 of the LDL receptor gene: identification of a new deletion mutation.

Theart, L; Kotze, M J; Langenhoven, E; Loubser, O; Peeters, A V; Lintott, C J; Scott, R S.

Affiliation

Theart L; Department of Human Genetics, Faculty of Medicine, University of Stellenbosch, Tygerberg, South Africa.

J Med Genet ; 32(5): 379-82, 1995 May.

Article in En | MEDLINE | ID: mdl-7616546

Subject(s)

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Receptors, LDL / Sequence Deletion / Hyperlipoproteinemia Type II Type of study: Diagnostic_studies / Screening_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Oceania Language: En Journal: J Med Genet Year: 1995 Document type: Article Affiliation country: Country of publication:

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Receptors, LDL / Sequence Deletion / Hyperlipoproteinemia Type II Type of study: Diagnostic_studies / Screening_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Oceania Language: En Journal: J Med Genet Year: 1995 Document type: Article Affiliation country: Country of publication: