WordNet

(genetics) any event that changes genetic structure; any alteration in the inherited nucleic acid sequence of the genotype of an organism (同)genetic mutation, chromosomal_mutation
a change or alteration in form or qualities
(genetics) a segment of DNA that is involved in producing a polypeptide chain; it can include regions preceding and following the coding DNA as well as introns between the exons; it is considered a unit of heredity; "genes were formerly called factors" (同)cistron, factor
informal term for information; "give me the gen on your new line of computers"

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1. 糖尿病および遺伝的糖尿病症候群の分類 classification of diabetes mellitus and genetic diabetic syndromes
2. 幼児の持続性高インスリン血症性低血糖症の病因、臨床的特徴、および診断 pathogenesis clinical features and diagnosis of persistent hyperinsulinemic hypoglycemia of infancy
3. 2型糖尿病の病因 pathogenesis of type 2 diabetes mellitus
4. 乳児の持続性高インスリン血症性低血糖症の治療および合併症 treatment and complications of persistent hyperinsulinemic hypoglycemia of infancy
5. 新生児高血糖 neonatal hyperglycemia

Mutational analysis of ABCC8, KCNJ11, GLUD1, HNF4A and GCK genes in 30 Chinese patients with congenital hyperinsulinism

Sang Yanmei,Xu Zidi,Liu Min,Yan Jie,Wu Yujun,Zhu Cheng,Ni Guichen
Endocrine Journal 61(9), 901-910, 2014
… All exons of the adenosine triphosphate (ATP)-sensitive potassium channel (KATP channel) genes KCNJ11 and ABCC8, the hepatocyte nuclear factor 4 α (HNF4A) gene, and the Glucokinase (GCK) gene as well as exons 6 and 7 and 10-12 of the glutamate dehydrogenase 1 (GLUD1) gene were amplified from genomic DNA and directly sequenced. … We found a novel de novo ABCC8 mutation, p. …
NAID 130004690921

A Novel Mutation of the Glucokinase Gene in Maturityonset Diabetes of the Young Type 2 (MODY2)

島田典生,武者廣隆
医療 51(12), 569-573, 1997
インスリン非依存型糖尿病(NIDDM)では, インスリン分泌の低下とインスリン作用の障害がみられ, その発症には環境因子に加えて遺伝因子が重要な働きをもっていると考えられる. 近年の分子生物学の進歩により, 糖尿病を引き起こす可能性のある遺伝子(候補遺伝子)のいくつかが単離され, これらの遺伝子と糖尿病との関連を検索することが可能となり, 一部の糖尿病に関して遺伝子変異と糖尿病との関係が明らかとな …
NAID 130004107596

リンク元	「グルコキナーゼ遺伝子異常」