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NALCN Dysfunction as a Cause of Disordered Respiratory Rhythm With Central Apnea.
Campbell, Jamie; FitzPatrick, David R; Azam, Tara; Gibson, Neil A; Somerville, Laura; Joss, Shelagh K; Urquhart, Don S.
Afiliação
  • Campbell J; Department of Clinical Genetics, Centre for Genomic and Experimental Medicine and jamie.campbell@nhs.net.
  • FitzPatrick DR; Medical Research Council Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.
  • Azam T; South-East Scotland Regional Genetics Laboratories, Western General Hospital, Edinburgh, United Kingdom.
  • Gibson NA; Department of Respiratory and Sleep Medicine, Royal Hospital for Children, Glasgow, United Kingdom.
  • Somerville L; Specialist Children's Services, The West Centre, Glasgow, United Kingdom.
  • Joss SK; West of Scotland Clinical Genetics Service, Queen Elizabeth University Hospital, Govan, United Kingdom.
  • Urquhart DS; Department of Pediatric Respiratory and Sleep Medicine, Royal Hospital for Sick Children, Edinburgh, United Kingdom.
Pediatrics ; 141(Suppl 5): S485-S490, 2018 04.
Article em En | MEDLINE | ID: mdl-29610177
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Canais de Sódio / Deficiências do Desenvolvimento / Apneia do Sono Tipo Central / Hipotonia Muscular / Mutação Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Canais de Sódio / Deficiências do Desenvolvimento / Apneia do Sono Tipo Central / Hipotonia Muscular / Mutação Idioma: En Ano de publicação: 2018 Tipo de documento: Article