Literature DB >> 16216955

Significance of recurrent mutations in the myofibrillogenesis regulator 1 gene.

Ana Djarmati, Marina Svetel, Dragana Momcilovic, Vladimir Kostic, Christine Klein.   

Abstract

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Year:  2005        PMID： 16216955     DOI： 10.1001/archneur.62.10.1641-a

Source DB:  PubMed          Journal:  Arch Neurol        ISSN： 0003-9942


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  3 in total

1.  Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias.

Authors:  Dolores Martínez-Rubio; Isabel Hinarejos; Paula Sancho; Nerea Gorría-Redondo; Raquel Bernadó-Fonz; Cristina Tello; Clara Marco-Marín; Itxaso Martí-Carrera; María Jesús Martínez-González; Ainhoa García-Ribes; Raquel Baviera-Muñoz; Isabel Sastre-Bataller; Irene Martínez-Torres; Anna Duat-Rodríguez; Patrícia Janeiro; Esther Moreno; Leticia Pías-Peleteiro; Mar O'Callaghan Gordo; Ángeles Ruiz-Gómez; Esteban Muñoz; Maria Josep Martí; Ana Sánchez-Monteagudo; Candela Fuster; Amparo Andrés-Bordería; Roser Maria Pons; Silvia Jesús-Maestre; Pablo Mir; Vincenzo Lupo; Belén Pérez-Dueñas; Alejandra Darling; Sergio Aguilera-Albesa; Carmen Espinós
Journal:  Int J Mol Sci       Date:  2022-10-06       Impact factor: 6.208

Review 2.  The genetics of dystonia: new twists in an old tale.

Authors:  Gavin Charlesworth; Kailash P Bhatia; Nicholas W Wood
Journal:  Brain       Date:  2013-06-17       Impact factor: 13.501

3.  The PNKD gene is associated with Tourette Disorder or Tic disorder in a multiplex family.

Authors:  N Sun; C Nasello; L Deng; N Wang; Y Zhang; Z Xu; Z Song; K Kwan; R A King; Z P Pang; J Xing; G A Heiman; J A Tischfield
Journal:  Mol Psychiatry       Date:  2017-09-12       Impact factor: 15.992
  3 in total

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