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Charcot-Marie-Tooth disease type 2S: identical novel missense mutation of IGHMBP2 gene in two unrelated families.
Chandrasekharan, Soumya V; Nair, Sruthi S; Ganapathy, Aparna; Mannan, Ashraf U; Sundaram, Soumya.
Afiliação
  • Chandrasekharan SV; Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Thiruvananthapuram, Kerala, India.
  • Nair SS; Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Thiruvananthapuram, Kerala, India.
  • Ganapathy A; Strand Life Sciences, Bangalore, India.
  • Mannan AU; Strand Life Sciences, Bangalore, India.
  • Sundaram S; Pediatric Neurology and Neurodevelopmental Disorders, Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Thiruvananthapuram, 695011, Kerala, India. ssdr.soumya@gmail.com.
Neurol Sci ; 43(1): 719-722, 2022 01.
Article em En | MEDLINE | ID: mdl-34668123
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Doença de Charcot-Marie-Tooth / Proteínas de Ligação a DNA Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Doença de Charcot-Marie-Tooth / Proteínas de Ligação a DNA Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article