Identification of novel mutations in patients with coffin-lowry syndrome by a denaturing HPLC-based assay

Research output: Contribution to journalArticle

4 Citations (Scopus)
Original languageEnglish
Pages (from-to)2356-2358
Number of pages3
JournalClinical Chemistry
Volume51
Issue number12
DOIs
Publication statusPublished - Dec 2005

ASJC Scopus subject areas

  • Clinical Biochemistry

Cite this

@article{1fc4f1dbc1944da9956b6a10010928e8,
title = "Identification of novel mutations in patients with coffin-lowry syndrome by a denaturing HPLC-based assay",
author = "Michele Falco and Corrado Romano and Antonino Alberti and Donatella Greco and Carmela Scuderi and Emanuela Avola and Pinella Failla and Serena Belli and Tolmie, {John L.} and Silvestra Amata and Marco Fichera",
year = "2005",
month = "12",
doi = "10.1373/clinchem.2005.056036",
language = "English",
volume = "51",
pages = "2356--2358",
journal = "Clinical Chemistry",
issn = "0009-9147",
publisher = "American Association for Clinical Chemistry Inc.",
number = "12",

}

TY - JOUR

T1 - Identification of novel mutations in patients with coffin-lowry syndrome by a denaturing HPLC-based assay

AU - Falco, Michele

AU - Romano, Corrado

AU - Alberti, Antonino

AU - Greco, Donatella

AU - Scuderi, Carmela

AU - Avola, Emanuela

AU - Failla, Pinella

AU - Belli, Serena

AU - Tolmie, John L.

AU - Amata, Silvestra

AU - Fichera, Marco

PY - 2005/12

Y1 - 2005/12

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U2 - 10.1373/clinchem.2005.056036

DO - 10.1373/clinchem.2005.056036

M3 - Article

C2 - 16306095

AN - SCOPUS:28044468828

VL - 51

SP - 2356

EP - 2358

JO - Clinical Chemistry

JF - Clinical Chemistry

SN - 0009-9147

IS - 12

ER -