Literature DB >> 25487718

Incomplete penetrance in limb-girdle muscular dystrophy type 1F.

Marina Fanin1, Enrico Peterle1, Chiara Fritegotto1, Anna C Nascimbeni1, Elisabetta Tasca2, Annalaura Torella3,4, Vincenzo Nigro3,4, Corrado Angelini1,2.   

Abstract

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Year:  2015        PMID： 25487718     DOI： 10.1002/mus.24539

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN： 0148-639X            Impact factor:   3.217


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  4 in total

Review 1.  Karyopherins in cancer.

Authors:  Tolga Çağatay; Yuh Min Chook
Journal:  Curr Opin Cell Biol       Date:  2018-02-04       Impact factor: 8.382

2.  Novel mutation in TNPO3 causes congenital limb-girdle myopathy with slow progression.

Authors:  Anna Vihola; Johanna Palmio; Olof Danielsson; Sini Penttilä; Daniel Louiselle; Sara Pittman; Conrad Weihl; Bjarne Udd
Journal:  Neurol Genet       Date:  2019-05-02

3.  Circulating miR-206 as a Biomarker for Patients Affected by Severe Limb Girdle Muscle Dystrophies.

Authors:  Valentina Pegoraro; Corrado Angelini
Journal:  Genes (Basel)       Date:  2021-01-12       Impact factor: 4.096

Review 4.  LGMD D2 TNPO3-Related: From Clinical Spectrum to Pathogenetic Mechanism.

Authors:  Roberta Costa; Maria Teresa Rodia; Serafina Pacilio; Corrado Angelini; Giovanna Cenacchi
Journal:  Front Neurol       Date:  2022-03-04       Impact factor: 4.003
  4 in total

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