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A case report of concurrent occurrence of two inherited axonopathies within a family: the benefit of whole-exome sequencing.
Sadr, Zahra; Rohani, Mohammad; Jamali, Payman; Alavi, Afagh.
Afiliação
  • Sadr Z; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Rohani M; Department of Neurology, Hazrat Rasool Hospital, School of Medicines, Iran University of Medical Sciences, Tehran, Iran.
  • Jamali P; Genetic Counseling Center, Shahroud, Iran.
  • Alavi A; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Int J Neurosci ; : 1-6, 2023 Sep 15.
Article em En | MEDLINE | ID: mdl-37712628
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Int J Neurosci Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Int J Neurosci Ano de publicação: 2023 Tipo de documento: Article