Quantitative and Sensitive Detection of GNAS Mutations Causing McCune-Albright Syndrome with Next Generation Sequencing

PLoS ONE

Volumn 8, Issue 3, 2013, Pages

  Narumi, Satoshi ^a   Matsuo, Kumihiro ^b   Ishii, Tomohiro ^a   Tanahashi, Yusuke ^b   Hasegawa, Tomonobu ^a  

^a KEIO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b ASAHIKAWA MEDICAL COLLEGE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

GUANINE NUCLEOTIDE BINDING PROTEIN ALPHA SUBUNIT; PEPTIDE NUCLEIC ACID;

ALBRIGHT SYNDROME; AMPLICON; ARTICLE; CLINICAL ARTICLE; DNA DETERMINATION; EXON; FEMALE; GENE ACTIVATION; GENE LOCUS; GENE SEQUENCE; GENETIC PROCEDURES; GUANINE NUCLEOTIDE BINDING PROTEIN ALPHA SUBUNIT GENE; HUMAN; HUMAN CELL; INTERMETHOD COMPARISON; LIMIT OF DETECTION; MALE; MOLECULAR CLONING; MUTATIONAL ANALYSIS; NEXT GENERATION SEQUENCING; NUCLEIC ACID ANALYSIS; QUANTITATIVE ANALYSIS; RELIABILITY; SENSITIVITY ANALYSIS; SEQUENCE ANALYSIS; SOMATIC MUTATION; WILD TYPE;

FEMALE; FIBROUS DYSPLASIA, POLYOSTOTIC; GTP-BINDING PROTEIN ALPHA SUBUNITS, GS; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; MALE; MUTATION; MUTATION RATE; REPRODUCIBILITY OF RESULTS; SENSITIVITY AND SPECIFICITY;

EID: 84875426448     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0060525     Document Type: Article

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