Mutation analysis of the FBN1 gene in patients with Marfan syndrome.

Methods in molecular medicine

Volumn 126, Issue , 2006, Pages 81-95

  Coucke, Paul ^a   Van Acker, Petra ^a   De Paepe, Anne ^a  

^a GHENT UNIVERSITY HOSPITAL   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIN BINDING PROTEIN; COMPLEMENTARY DNA; DNA; FIBRILLIN; MESSENGER RNA;

ARTICLE; BIOSYNTHESIS; CELL CULTURE; DNA DENATURATION; GENETICS; GENOME; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; ISOLATION AND PURIFICATION; MARFAN SYNDROME; METHODOLOGY; NUCLEIC ACID AMPLIFICATION; NUCLEOTIDE SEQUENCE;

CELLS, CULTURED; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; DNA; DNA MUTATIONAL ANALYSIS; DNA, COMPLEMENTARY; GENOME, HUMAN; HUMANS; MARFAN SYNDROME; MICROFILAMENT PROTEINS; NUCLEIC ACID AMPLIFICATION TECHNIQUES; NUCLEIC ACID DENATURATION; RNA, MESSENGER;

EID: 33846785888     PISSN: 15431894     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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