Glycogen branching enzyme deficiency in an infant with severe congenital hypotonia: an emerging diagnosis of muscle weakness in the perinatal period

التفاصيل البيبلوغرافية
العنوان: Glycogen branching enzyme deficiency in an infant with severe congenital hypotonia: an emerging diagnosis of muscle weakness in the perinatal period
المؤلفون: Andrés Nascimento, Rosaline Froissart, Isidro Ferrer, Cecilia Jimenez-Mallebrera, Jaume Colomer, Victoria Cusi, Montse Olivé, Marie-Odile Rolland, J. Corbera
المصدر: Histopathology. 54:765-768
بيانات النشر: Wiley, 2009.
سنة النشر: 2009
مصطلحات موضوعية: Glycogen Branching Enzyme Deficiency, Pediatrics, medicine.medical_specialty, Histology, business.industry, medicine, Muscle weakness, General Medicine, Congenital hypotonia, medicine.symptom, business, Perinatal period, Pathology and Forensic Medicine
تدمد: 1365-2559
0309-0167
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::ae2efdcd8ad0fa706995d86383b9ef54Test
https://doi.org/10.1111/j.1365-2559.2009.03281.xTest
حقوق: CLOSED
رقم الانضمام: edsair.doi...........ae2efdcd8ad0fa706995d86383b9ef54
قاعدة البيانات: OpenAIRE