WordNet

(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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[Clinical characteristics and genetic mutation analysis in a Hui family with Huntington disease].

Chen J, Lei J, Zhang XN.SourcePhysical Examination and Health Management Center, the First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, People's Republic of China.
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.Zhonghua Yi Xue Yi Chuan Xue Za Zhi.2011 Oct;28(5):493-5.
OBJECTIVE: To perform clinical analysis and gene diagnosis of Huntington disease (HD) in a Hui pedigree from Xinjiang.METHODS: The IT15 gene mutation of the Hui family was analyzed by touchdown PCR, molecular cloning and gene sequencing.RESULTS: The proband carried 46 CAG repeats. Pain in bilateral
PMID 21983719

Co-segregation of Huntington disease and hereditary spastic paraplegia in 4 generations.

Panas M, Karadima G, Kalfakis N, Vassilopoulos D.SourceNeurogenetics Unit, Department of Neurology, Eginition Hospital, University of Athens, Athens, Greece. mpanas@med.uoa.gr
The neurologist.Neurologist.2011 Jul;17(4):211-2.
INTRODUCTION: Huntington disease (HD) is an autosomal dominant neurodegenerative disease characterized by choreic hyperkinesias, cognitive decline, and psychiatric manifestations, caused by an increased number of CAG repeats in the IT15 gene on chromosome 4p16.3. Silver syndrome is a rare autosomal
PMID 21712667