Next generation sequencing in the diagnosis of inherited cardiac disorders

被引：0
|
作者：
Benedetti, S. [1 ]
Merella, S. [1 ,2 ]
Di Resta, C. [3 ]
Foglio, A. [1 ]
Zanussi, M. [1 ]
Pucci, P. [3 ]
Pipitone, G. [1 ]
Pappone, C. [4 ]
Sala, S. [5 ]
Spoladore, R. [6 ]
Ferrari, M. [1 ,3 ,7 ]
Carrera, P. [1 ,7 ]
机构：
[1] IRCCS S Raffaele, Clin Mol Biol Lab, Milan, Italy
[2] IRCCS San Raffaele, Ctr Translat Genom & Bioinformat, Milan, Italy
[3] Univ Vita San Salute San Raffaele, Milan, Italy
[4] Univ Milan, Dept Arrhythmol, IRCCS Policlin San Donato, Milan, Italy
[5] IRCCS San Raffaele, Dept Arrhythmol, Milan, Italy
[6] IRCCS San Raffaele, Cardiol Unit, Referral Ctr Hypertroph Cardiomyopathy, Milan, Italy
[7] IRCCS San Raffaele, Unit Genom Human Dis Diag, Milan, Italy
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2018年 / 26卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
P05.14B
引用
收藏
页码：263 / 264
页数：2
相关论文
共 50 条
  • [31] Next-generation sequencing approaches for the diagnosis of skeletal muscle disorders
    Nigro, Vincenzo
    Savarese, Marco
    CURRENT OPINION IN NEUROLOGY, 2016, 29 (05) : 621 - 627
  • [32] Application of next generation sequencing in the diagnosis of hereditary connective tissue disorders
    Pope, M. K.
    Johnsen, H. M.
    Rypdal, K. B.
    Sejersted, Y.
    Paus, B.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 520 - 520
  • [33] NEXT GENERATION SEQUENCING IN THE DIAGNOSIS OF RED BLOOD CELL MEMBRANE DISORDERS
    van Wijk, Richard
    Vogel, Maartje
    Elferink, Martin
    Nijman, Ies
    Cuppen, Edwin
    van Solinge, Wouter
    van Amstel, Hans Kristian Ploos
    van der Zwaag, Bert
    INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, 2014, 36 : 18 - 18
  • [34] Added value of next generation sequencing (NGS) in the diagnosis of neuromuscular disorders
    Brignol, Tuy Nga
    M S-MEDECINE SCIENCES, 2016, 32 : 47 - 48
  • [35] Next generation sequencing provides diagnosis for multiple foetal akinesia disorders
    Todd, E. J.
    Ong, R.
    Barnett, C.
    Slee, J.
    Ryan, M.
    Howel, K.
    Sivadorai, P.
    Davis, M. R.
    Allcock, R. J. N.
    Laing, N. G.
    Ravenscroft, G.
    NEUROMUSCULAR DISORDERS, 2013, 23 (9-10) : 787 - 788
  • [36] Implementation of next generation sequencing for clinical molecular diagnosis of mitochondrial disorders
    Zhang, Victor Wei
    Cui, Hong
    Wong, Lee-Jun
    MITOCHONDRION, 2012, 12 (05) : 555 - 556
  • [37] Inherited Cancer in the Age of Next-Generation Sequencing
    Price, Kristin S.
    Svenson, Ashley
    King, Elisabeth
    Ready, Kaylene
    Lazarin, Gabriel A.
    BIOLOGICAL RESEARCH FOR NURSING, 2018, 20 (02) : 192 - 204
  • [38] EVALUATING NEXT GENERATION SEQUENCING PANELS FOR INHERITED NEUROPATHIES
    Newhall, A.
    Hanson-Kahn, A. K.
    Dalton, J.
    Siskind, C.
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2015, 20 (02) : 200 - 200
  • [39] Inherited platelet disorders: Insight from platelet genomics using next-generation sequencing
    Maclachlan, Annabel
    Watson, Steve P.
    Morgan, Neil V.
    PLATELETS, 2017, 28 (01) : 14 - 19
  • [40] Challenges using diagnostic next-generation sequencing in the clinical environment for inherited retinal disorders
    Davies, Wayne I. L.
    PERSONALIZED MEDICINE, 2014, 11 (01) : 99 - 111
12345