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A first CLN6 variant case of late infantile neuronal ceroid lipofuscinosis caused by a homozygous mutation in a boy from China: a case report.
Sun, Guilian; Yao, Fang; Tian, Zhuoling; Ma, Tianjiao; Yang, Zhiliang.
Afiliação
  • Sun G; Department of Pediatrics, The First Hospital of China Medical University, No. 155 Nanjing North Street, Heping District, Shenyang, 110001, Liaoning Province, People's Republic of China.
  • Yao F; Department of Pediatrics, The First Hospital of China Medical University, No. 155 Nanjing North Street, Heping District, Shenyang, 110001, Liaoning Province, People's Republic of China.
  • Tian Z; Department of Pediatrics, The First Hospital of China Medical University, No. 155 Nanjing North Street, Heping District, Shenyang, 110001, Liaoning Province, People's Republic of China.
  • Ma T; Department of Pediatrics, The First Hospital of China Medical University, No. 155 Nanjing North Street, Heping District, Shenyang, 110001, Liaoning Province, People's Republic of China.
  • Yang Z; Department of Pediatrics, The First Hospital of China Medical University, No. 155 Nanjing North Street, Heping District, Shenyang, 110001, Liaoning Province, People's Republic of China. sizhewujiu@163.com.
BMC Med Genet ; 19(1): 177, 2018 10 01.
Article em En | MEDLINE | ID: mdl-30285654

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Convulsões / Mutação de Sentido Incorreto / Leucoencefalopatias / Proteínas de Membrana / Lipofuscinoses Ceroides Neuronais Tipo de estudo: Diagnostic_studies Limite: Adult / Child, preschool / Female / Humans / Male Idioma: En Revista: BMC Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Convulsões / Mutação de Sentido Incorreto / Leucoencefalopatias / Proteínas de Membrana / Lipofuscinoses Ceroides Neuronais Tipo de estudo: Diagnostic_studies Limite: Adult / Child, preschool / Female / Humans / Male Idioma: En Revista: BMC Med Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article