Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes

Journal of the American Society of Nephrology

Volumn 13, Issue 1, 2002, Pages 65-74

  Arrondel, C ^a   Vodovar, N ^a   Knebelmann, B ^a   Grunfeld J ^a   Gubler, M ^a   Antignac, C ^a   Heidet, L ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; ASPARAGINE; ASPARTIC ACID; GENE PRODUCT; GLUTAMINE; LEUCINE; LYSINE; MYOSIN HEAVY CHAIN; MYOSIN HEAVY CHAIN IIA; PROTEIN MYH9; SERINE; UNCLASSIFIED DRUG;

ARTICLE; CHROMOSOME 22Q; CLINICAL ARTICLE; CODON; CONTROLLED STUDY; ENDOTHELIUM; EXON; FECHTNER SYNDROME; FEMALE; FETUS; GENE EXPRESSION; GENETIC ANALYSIS; GENETIC LINKAGE; GLOMERULUS; HUMAN; HUMAN TISSUE; KIDNEY; KIDNEY DEVELOPMENT; KIDNEY EPITHELIUM; KIDNEY TUBULE; MALE; MAY HEGGLIN ANOMALY; MISSENSE MUTATION; NEPHRITIS; NEPHROTIC SYNDROME; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; SEBASTIAN SYNDROME; SINGLE STRAND CONFORMATION POLYMORPHISM; THROMBOCYTOPENIA;

EID: 0036138503     PISSN: 10466673     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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