Literature DB >> 22190360

SIGMAR1 mutations, genetic heterogeneity at the chromosome 9p locus, and the expanding etiological diversity of amyotrophic lateral sclerosis.

Faisal Fecto, Teepu Siddique.   

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Year:  2011        PMID： 22190360     DOI： 10.1002/ana.22648

Source DB:  PubMed          Journal:  Ann Neurol        ISSN： 0364-5134            Impact factor:   10.422


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  4 in total

1.  Molecular evaluation of human ubiquilin 2 gene PXX domain in familial frontotemporal dementia patients.

Authors:  Isabel Hernández; Anna Espinosa; Luis Miguel Real; Jose Jorge Galán; Ana Mauleón; Maiteé Rosende Roca; Lluís Tárraga; Agustín Ruiz; Mercè Boada
Journal:  J Neurol       Date:  2012-06-24       Impact factor: 4.849

Review 2.  Sigma-1 receptor chaperones in neurodegenerative and psychiatric disorders.

Authors:  Shang-Yi A Tsai; Michael J Pokrass; Neal R Klauer; Nicole E De Credico; Tsung-Ping Su
Journal:  Expert Opin Ther Targets       Date:  2014-10-21       Impact factor: 6.902

3.  In silico analysis of SIGMAR1 variant (rs4879809) segregating in a consanguineous Pakistani family showing amyotrophic lateral sclerosis without frontotemporal lobar dementia.

Authors:  Muhammad Ikram Ullah; Arsalan Ahmad; Syed Irfan Raza; Ali Amar; Amjad Ali; Attya Bhatti; Peter John; Aisha Mohyuddin; Wasim Ahmad; Muhammad Jawad Hassan
Journal:  Neurogenetics       Date:  2015-07-24       Impact factor: 2.660

4.  Genotype-phenotype relationship in hereditary amyotrophic lateral sclerosis.

Authors:  Satoshi Yamashita; Yukio Ando
Journal:  Transl Neurodegener       Date:  2015-07-24       Impact factor: 8.014
  4 in total

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