Mosaicism - Switch or spectrum?

Science

Volumn 330, Issue 6000, 2010, Pages 46-47

  Davis, Brian R ^a   Candotti, Fabio ^b  

^a UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

^b NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

KERATIN; CYTOKERATIN 10; KRT10 PROTEIN, HUMAN; MUTANT PROTEIN;

GENETIC ANALYSIS; MUTATION; PROTEIN; RECOMBINATION; SKIN DISORDER;

CELL POPULATION; CONGENITAL ICHTHYOSIFORM ERYTHRODERMA; DNA DAMAGE; FRAMESHIFT MUTATION; GENE THERAPY; HUMAN; MISSENSE MUTATION; MOSAICISM; PRIORITY JOURNAL; REVERTANT; SHORT SURVEY; SOMATIC CELL GENETICS; SOMATIC MUTATION; CHROMOSOME 17; GENETIC RECOMBINATION; GENETIC SELECTION; GENETICS; HETEROZYGOSITY LOSS; METABOLISM; MITOSIS; NOTE; PATHOLOGY; SKIN;

CHROMOSOMES, HUMAN, PAIR 17; FRAMESHIFT MUTATION; HUMANS; ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL; KERATIN-10; LOSS OF HETEROZYGOSITY; MITOSIS; MOSAICISM; MUTANT PROTEINS; RECOMBINATION, GENETIC; SELECTION, GENETIC; SKIN;

EID: 77957327728     PISSN: 00368075     EISSN: 10959203     Source Type: Journal    
DOI: 10.1126/science.1195991     Document Type: Short Survey

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