SCOPUS 정보 검색 플랫폼

Molecular Cell

Volumn 53, Issue 1, 2014, Pages 1-3

To switch or not to switch: At the origin of repeat expansion disease

(2) Mirkin, Ekaterina V a Mirkin, Sergei M b

a HARVARD UNIVERSITY (United States)

b TUFTS UNIVERSITY (United States)

Author keywords

[No Author keywords available]

Indexed keywords

REPETITIVE DNA; FMR1 PROTEIN, HUMAN; FRAGILE X MENTAL RETARDATION PROTEIN;

AMYOTROPHIC LATERAL SCLEROSIS; CELL DIFFERENTIATION; DNA RECOMBINATION; DNA REPAIR; DNA REPLICATION; DNA REPLICATION ORIGIN; DNA STRAND; EMBRYO DEVELOPMENT; FRAGILE X SYNDROME; GENE EXPRESSION; GENETIC DISORDER; GENETIC PREDISPOSITION; HUMAN; HUNTINGTON CHOREA; MYOTONIC DYSTROPHY; SHORT SURVEY; EMBRYOLOGY; EMBRYONIC STEM CELL; GENE LOCUS; METABOLISM; TRINUCLEOTIDE REPEAT;

DNA REPLICATION; EMBRYONIC STEM CELLS; FRAGILE X MENTAL RETARDATION PROTEIN; FRAGILE X SYNDROME; GENETIC LOCI; HUMANS; TRINUCLEOTIDE REPEATS;

EID: 84892149837 PISSN: 10972765 EISSN: 10974164 Source Type: Journal
DOI: 10.1016/j.molcel.2013.12.021 Document Type: Short Survey

Times cited : (23)

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