Continued lessons from the INS gene: An intronic mutation causing diabetes through a novel mechanism

Journal of Medical Genetics

Volumn 52, Issue 9, 2015, Pages 612-616

  Carmody, David ^a   Park, Soo Young ^a   Ye, Honggang ^a   Perrone, Marie E ^a   Alkorta Aranburu, G ^a   Highland, Heather M ^b   Hanis, Craig L ^b   Philipson, Louis H ^a   Bell, Graeme I ^a   Greeley, Siri Atma W ^a  

^a UNIVERSITY OF CHICAGO   (United States)

^b UNIVERSITY OF TEXAS SCHOOL OF PUBLIC HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMYLIN; C PEPTIDE; GENOMIC DNA; INSULIN; MESSENGER RNA; HUMAN INSULIN;

ANIMAL CELL; ARTICLE; CELL LINE; CONTROLLED STUDY; ECHOGRAPHY; FEMALE; GENE CONSTRUCT; GENE EXPRESSION; GENE MUTATION; GENE SEQUENCE; HUMAN; HUMAN CELL; INTRON; MALE; NEWBORN; NEWBORN DIABETES MELLITUS; NONHUMAN; PRIORITY JOURNAL; RAT; SEQUENCE ANALYSIS; CASE REPORT; DIABETES MELLITUS; DNA SEQUENCE; GENETICS; INFANT; MUTATION;

DIABETES MELLITUS; HUMANS; INFANT; INSULIN, REGULAR, HUMAN; INTRONS; MUTATION; SEQUENCE ANALYSIS, DNA;

EID: 84945454339     PISSN: 00222593     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmedgenet-2015-103220     Document Type: Article

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