Absence of mutations in human ubiquitin fusion-degradation protein gene in tetralogy of Fallot

Journal of Molecular Medicine

Volumn 79, Issue 5-6, 2001, Pages 338-342

  Chung, Ming yi ^a   Lu, Jen Her ^a,b   Weng, Ying Yen ^a   Hwang, BeTau ^a,b  

^a TAIPEI VETERANS GENERAL HOSPITAL   (Taiwan)

^b NATIONAL YANG MING UNIVERSITY   (Taiwan)

Author keywords

Mutation analysis; Tetralogy of Fallot; UFD1L gene

Indexed keywords

NUCLEOTIDE; UBIQUITIN;

ARTICLE; CHROMOSOME 22Q; DNA FLANKING REGION; FALLOT TETRALOGY; GENE DELETION; GENE MUTATION; GENE SEQUENCE; HEART SEPTUM DEFECT; HUMAN; HUMAN CELL; INTRON; LUNG ATRESIA; MAJOR CLINICAL STUDY; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

AMINO ACID SEQUENCE; BASE SEQUENCE; CHROMOSOMES, HUMAN, PAIR 22; DNA MUTATIONAL ANALYSIS; EXONS; GENE DOSAGE; GENETIC SCREENING; HETERODUPLEX ANALYSIS; HUMANS; INTRONS; MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEINS; TETRALOGY OF FALLOT;

EID: 0034933113     PISSN: 09462716     EISSN: None     Source Type: Journal    
DOI: 10.1007/s001090100213     Document Type: Article

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