Detection of Rare Somatic GNAS Mutation in McCune-Albright Syndrome Using a Novel Peptide Nucleic Acid Probe in a Single Tube.

Lo, Fu-Sung; Chen, Tai-Long; Chiou, Chiuan-Chian

Lo, Fu-Sung; Chen, Tai-Long; Chiou, Chiuan-Chian.

Lo FS; Division of Pediatric Endocrinology & Genetics, Chang Gung Memorial Hospital, Linkou, Taoyuan 333, Taiwan. lofusu@cgmh.org.tw.
Chen TL; School of Medicine, College of Medicine, Chang Gung University, Taoyuan 333, Taiwan. lofusu@cgmh.org.tw.
Chiou CC; Molecular Medicine Research Center, College of Medicine, Chang Gung University, Taoyuan 333, Taiwan. tl.chen@outlook.com.

Molecules ; 22(11)2017 Nov 01.

Article en En | MEDLINE | ID: mdl-29104223

Asunto(s)

Cromograninas/genética; Displasia Fibrosa Poliostótica/genética; Subunidades alfa de la Proteína de Unión al GTP Gs/genética; Ácidos Nucleicos de Péptidos/química; Análisis Mutacional de ADN; Humanos; Mutación/genética

Palabras clave

GNAS mutation; McCune-Albright syndrome; peptide nucleic acid probe; sensitive detection

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cromograninas / Subunidades alfa de la Proteína de Unión al GTP Gs / Ácidos Nucleicos de Péptidos / Displasia Fibrosa Poliostótica Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Año: 2017 Tipo del documento: Article

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