Phenotypic Characterization of a Family With An In-frame Deletion in the DMD Gene and Variable Penetrance-Reference-Cited by-同舟云学术

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Phenotypic Characterization of a Family With An In-frame Deletion in the DMD Gene and Variable Penetrance

Published:2018-10-04 Issue:4 Volume:18 Page:246-251
ISSN:1566-5232
Container-title:Current Gene Therapy
language:en
Short-container-title:CGT

Author:

Perez-Sanchez Inmaculada¹,Sabater-Molina Maria¹,Rocamora Maria Elisa Nicolas²,Glover Guillermo³,Escudero Fuensanta⁴,de Mingo Casado Pedro⁵,Gimeno-Blanes Juan Ramon¹

Affiliation:

1. Inherited Cardiac Disease Unit, University Hospital Virgen de la Arrixaca, Murcia, Spain

2. Internal Medicine Department, University of Murcia. Murcia, Spain

3. Center of Clinical Genetics and Biochemistry, University Hospital Virgen de la Arrixaca, Murcia, Spain

4. Pediatrics Service, University Hospital Virgen de la Arrixaca, Murcia, Spain

5. Neurology Service, University Hospital, Virgen de la Arrixaca, Murcia, Spain

Publisher

Bentham Science Publishers Ltd.

Subject

Genetics(clinical),Drug Discovery,Genetics,Molecular Biology,Molecular Medicine

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Heart in Disguise: Unmasking a Novel Gene Deletion in Dilated Cardiomyopathy;Cureus;2024-02-28

2. Clinical Phenotypes of DMD Exon 51 Skip Equivalent Deletions: A Systematic Review;Journal of Neuromuscular Diseases;2020-06-02

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