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Filamin A mutation associated with normal reading skills and dyslexia in a family with periventricular heterotopia.
Reinstein, Eyal; Chang, Bernard S; Robertson, Stephen P; Rimoin, David L; Katzir, Tami.
Affiliation
  • Reinstein E; Medical Genetics Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA.
Am J Med Genet A ; 158A(8): 1897-901, 2012 Aug.
Article in En | MEDLINE | ID: mdl-22740120
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Full text: 1 Database: MEDLINE Main subject: Reading / Contractile Proteins / Dyslexia / Periventricular Nodular Heterotopia / Microfilament Proteins / Mutation Type of study: Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2012 Type: Article Affiliation country: United States
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Full text: 1 Database: MEDLINE Main subject: Reading / Contractile Proteins / Dyslexia / Periventricular Nodular Heterotopia / Microfilament Proteins / Mutation Type of study: Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2012 Type: Article Affiliation country: United States