Deletion mapping in Alport syndrome and Alport syndrome-diffuse leiomyomatosis reveals potential mechanisms of visceral smooth muscle overgrowth.

Human mutation

Volumn 22, Issue 5, 2003, Pages 419-

  Thielen, Beth K ^a   Barker, David F ^a   Nelson, Raoul D ^a   Zhou, Jing ^a   Kren, Stefan M ^a   Segal, Yoav ^a  

^a UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COL4A5 PROTEIN, HUMAN; COLLAGEN TYPE 4;

ARTICLE; CHILD; CHROMOSOME MAP; FEMALE; GENE DELETION; GENE EXPRESSION REGULATION; GENETICS; HUMAN; LEIOMYOMATOSIS; MALE; MOLECULAR GENETICS; NEPHRITIS; NUCLEOTIDE SEQUENCE; PATHOLOGY; SEQUENCE ALIGNMENT; SMOOTH MUSCLE; VISCERA; X CHROMOSOME;

BASE SEQUENCE; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, X; COLLAGEN TYPE IV; FEMALE; GENE EXPRESSION REGULATION, NEOPLASTIC; HUMANS; LEIOMYOMATOSIS; MALE; MOLECULAR SEQUENCE DATA; MUSCLE, SMOOTH; NEPHRITIS, HEREDITARY; SEQUENCE ALIGNMENT; SEQUENCE DELETION; VISCERA;

EID: 2142853616     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9191     Document Type: Article

References (0)