Your browser doesn't support javascript.
loading
Expanding phenotype of mitochondrial depletion syndrome in association with TWNK mutations.
Sukhudyan, Biayna; Gevorgyan, Ani; Sarkissian, Ashot; Boltshauser, Eugen.
  • Sukhudyan B; Department of Pediatric Neurology, Arabkir Medical Center, 30 Mamikonyants str., 0014 Yerevan, Armenia. Electronic address: biayna_sukh@yahoo.com.
  • Gevorgyan A; Department of Pediatric Neurology, Arabkir Medical Center, 30 Mamikonyants str., 0014 Yerevan, Armenia. Electronic address: aniggr@mail.ru.
  • Sarkissian A; Department of Pediatrics, Yerevan State Medical University, 2 Koryun str., 0025 Yerevan, Armenia. Electronic address: ash_sarkissian@yahoo.com.
  • Boltshauser E; Department of Pediatric Neurology, University Children's Hospital, 75, Steinwiesstrasse, 8032 Zurich, Switzerland. Electronic address: eugen.boltshauser@bluewin.ch.
Eur J Paediatr Neurol ; 23(3): 537-540, 2019 May.
Article en En | MEDLINE | ID: mdl-30799093
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: ADN Helicasas / Enfermedades Mitocondriales / Proteínas Mitocondriales / Enfermedades Musculares Tipo de estudio: Risk_factors_studies Límite: Humans / Male Idioma: En Año: 2019 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: ADN Helicasas / Enfermedades Mitocondriales / Proteínas Mitocondriales / Enfermedades Musculares Tipo de estudio: Risk_factors_studies Límite: Humans / Male Idioma: En Año: 2019 Tipo del documento: Article