Identification of connexin43 (alpha1) gap junction gene mutations in patients with hypoplastic left heart syndrome by denaturing gradient gel electrophoresis (DGGE).

Dasgupta, C; Martinez, A M; Zuppan, C W; Shah, M M; Bailey, L L; Fletcher, W H

Dasgupta, C; Martinez, A M; Zuppan, C W; Shah, M M; Bailey, L L; Fletcher, W H.

Affiliation

Dasgupta C; Department of Biochemistry, School of Medicine, Loma Linda University, Loma Linda, CA 92354, USA.

Mutat Res ; 479(1-2): 173-86, 2001 Aug 08.

Article in En | MEDLINE | ID: mdl-11470490

Subject(s)

Connexin 43/genetics; Electrophoresis, Polyacrylamide Gel/methods; Gap Junctions/genetics; Hypoplastic Left Heart Syndrome/genetics; Mutation; Base Sequence; Child; Codon; Connexin 43/chemistry; DNA Mutational Analysis; Female; Formamides/pharmacology; Heart Transplantation; Humans; Infant; Infant, Newborn; Male; Molecular Sequence Data; Mutation, Missense; Peptides/chemistry; Phosphorylation; Protein Structure, Tertiary; Recombination, Genetic; Single-Blind Method; Temperature; Time Factors; Urea/pharmacology

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Collection: 01-internacional Database: MEDLINE Main subject: Gap Junctions / Connexin 43 / Hypoplastic Left Heart Syndrome / Electrophoresis, Polyacrylamide Gel / Mutation Type of study: Clinical_trials / Diagnostic_studies / Prognostic_studies Limits: Child / Female / Humans / Infant / Male / Newborn Language: En Journal: Mutat Res Year: 2001 Document type: Article Affiliation country: United States Country of publication: Netherlands

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