Literature DB >> 25219766

Making sense of the muscular dystrophies: diagnosis and treatment guideline for limb-girdle muscular dystrophy.

John D England1.   

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Year:  2014        PMID： 25219766     DOI： 10.1002/mus.24459

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


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  2 in total

1.  Linkage Study Revealed Complex Haplotypes in a Multifamily due to Different Mutations in CAPN3 Gene in an Iranian Ethnic Group.

Authors:  Marzieh Mojbafan; Seyed Hassan Tonekaboni; Maryam Abiri; Soudeh Kianfar; Ameneh Sarhadi; Yalda Nilipour; Javad Tavakkoly-Bazzaz; Sirous Zeinali
Journal:  J Mol Neurosci       Date:  2016-06-04       Impact factor: 3.444

2.  Homozygous nonsense mutation in SGCA is a common cause of limb-girdle muscular dystrophy in Assiut, Egypt.

Authors:  Hemakumar M Reddy; Sherifa A Hamed; Monkol Lek; Satomi Mitsuhashi; Elicia Estrella; Michael D Jones; Lane J Mahoney; Anna R Duncan; Kyung-Ah Cho; Daniel G Macarthur; Louis M Kunkel; Peter B Kang
Journal:  Muscle Nerve       Date:  2016-08-24       Impact factor: 3.217
  2 in total

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