Literature DB >> 11694554

Molecular and clinical study of two myotonic dystrophy homozygotes.

F Akbas1, P Serdaroglu, F Deymeer, F Aysal, N Erginel-Unaltuna.   

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Year:  2001        PMID： 11694554      PMCID： PMC1734760          DOI： 10.1136/jmg.38.11.e40

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  2 in total

1.  Improved method for molecular diagnosis of myotonic dystrophy type 1 (DM1).

Authors:  Nihan Erginel-Unaltuna; Fahri Akbas
Journal:  J Clin Lab Anal       Date:  2004       Impact factor: 2.352

2.  Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia.

Authors:  Pietro Fratta; Mark Poulter; Tammaryn Lashley; Jonathan D Rohrer; James M Polke; Jon Beck; Natalie Ryan; Davina Hensman; Sarah Mizielinska; Adrian J Waite; Mang-Ching Lai; Tania F Gendron; Leonard Petrucelli; Elizabeth M C Fisher; Tamas Revesz; Jason D Warren; John Collinge; Adrian M Isaacs; Simon Mead
Journal:  Acta Neuropathol       Date:  2013-07-02       Impact factor: 17.088
  2 in total

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