MED12, the mediator complex subunit 12 gene, is mutated at high frequency in uterine leiomyomas

Science

Volumn 334, Issue 6053, 2011, Pages 252-255

  Mäkinen, Netta ^a   Mehine, Miika ^a   Tolvanen, Jaana ^a   Kaasinen, Eevi ^a   Li, Yilong ^a   Lehtonen, Heli J ^a   Gentile, Massimiliano ^b   Yan, Jian ^c   Enge, Martin ^c   Taipale, Minna ^a,c   Aavikko, Mervi ^a   Katainen, Riku ^a   Virolainen, Elina ^d   Böhling, Tom ^d,e   Koski, Taru A ^a   Launonen, Virpi ^a   Sjöberg, Jari ^e   Taipale, Jussi ^a,c   Vahteristo, Pia ^a   Aaltonen, Lauri A ^a  

^a UNIVERSITY OF HELSINKI   (Finland)

^b Center for Science Ltd   (Finland)

^c SCIENCE FOR LIFE LABORATORY   (Sweden)

^d UNIVERSITY OF HELSINKI   (Finland)

^e HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; GENOMIC DNA;

COHORT ANALYSIS; ENZYME ACTIVITY; GENETIC ANALYSIS; MORBIDITY; MUTATION; TUMOR; WOMENS HEALTH;

ARTICLE; BENIGN TUMOR; CONTROLLED STUDY; EXOME; FEMALE; GENE EXPRESSION; GENE MUTATION; HUMAN; HUMAN TISSUE; LEIOMYOMA; LUJAN FRYNS SYNDROME; MAJOR CLINICAL STUDY; MEDIATOR COMPLEX SUBUNIT 12 GENE; MENTAL RETARDATION MALFORMATION SYNDROME; MYOMETRIUM; OPITZ SYNDROME; PRIORITY JOURNAL; SOMATIC MUTATION; UTERUS MYOMA; UTERUS TUMOR;

EID: 80054097980     PISSN: 00368075     EISSN: 10959203     Source Type: Journal    
DOI: 10.1126/science.1208930     Document Type: Article

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