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Genotype-Phenotype Correlations and Characterization of Medication Use in Inherited Myotonic Disorders.
Meyer, Alayne P; Roggenbuck, Jennifer; LoRusso, Samantha; Kissel, John; Smith, Rachel M; Kline, David; Arnold, W David.
Afiliação
  • Meyer AP; Division of Human Genetics, The Ohio State University, Columbus, OH, United States.
  • Roggenbuck J; Division of Human Genetics, The Ohio State University, Columbus, OH, United States.
  • LoRusso S; Department of Neurology, The Ohio State University, Columbus, OH, United States.
  • Kissel J; Department of Neurology, The Ohio State University, Columbus, OH, United States.
  • Smith RM; Department of Biomedical Informatics, Center for Biostatistics, The Ohio State University, Columbus, OH, United States.
  • Kline D; Department of Biomedical Informatics, Center for Biostatistics, The Ohio State University, Columbus, OH, United States.
  • Arnold WD; Department of Neurology, The Ohio State University, Columbus, OH, United States.
Front Neurol ; 11: 593, 2020.
Article em En | MEDLINE | ID: mdl-32670189

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article