Identification of LMX1B gene point mutations in italian patients affected with Nail-Patella syndrome.

International journal of molecular medicine

Volumn 4, Issue 3, 1999, Pages 285-290

  Seri, M ^a   Melchionda, S ^a   Dreyer, S ^a   Marini, M ^a   Carella, M ^a   Cusano, R ^a   Piemontese, M R ^a   Caroli, F ^a   Silengo, M ^a   Zelante, L ^a   Romeo, G ^a   Ravazzolo, R ^a   Gasparini, P ^a   Lee, B ^a  

^a G GASLINI INSTITUTE   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; HOMEODOMAIN PROTEIN; LIM HOMEOBOX TRANSCRIPTION FACTOR 1 BETA; PRIMER DNA; TRANSCRIPTION FACTOR;

ALTERNATIVE RNA SPLICING; ARTICLE; ETHNOLOGY; GENE EXPRESSION REGULATION; GENETICS; GLAUCOMA; HAPLOTYPE; HUMAN; ITALY; KIDNEY; NAIL PATELLA SYNDROME; NUCLEOTIDE SEQUENCE; POINT MUTATION; PRENATAL DEVELOPMENT; SINGLE STRAND CONFORMATION POLYMORPHISM;

ALTERNATIVE SPLICING; BASE SEQUENCE; DNA PRIMERS; DNA, COMPLEMENTARY; GENE EXPRESSION REGULATION; GLAUCOMA; HAPLOTYPES; HOMEODOMAIN PROTEINS; HUMANS; ITALY; KIDNEY; NAIL-PATELLA SYNDROME; POINT MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; TRANSCRIPTION FACTORS;

MLCS; MLOWN;

EID: 0033192624     PISSN: 11073756     EISSN: None     Source Type: Journal    
DOI: 10.3892/ijmm.4.3.285     Document Type: Article

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