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P184 – 2022 The brain-lung-thyroid syndrome as a rare cause of chorea: case report of a novel mutation in the thyroid transcription factor-1 (TITF-1) gene

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العنوان: P184 – 2022 The brain-lung-thyroid syndrome as a rare cause of chorea: case report of a novel mutation in the thyroid transcription factor-1 (TITF-1) gene
المؤلفون: Gunnar M. Buyse, N Reynaert, I Francois, G de Bruyn, Nathalie Goemans, L. De Waele, L Wouters, Lieven Lagae, Katrien Jansen
المصدر: European Journal of Paediatric Neurology. 17:S104
بيانات النشر: Elsevier BV, 2013.
سنة النشر: 2013
مصطلحات موضوعية: medicine.medical_specialty, business.industry, Thyroid Transcription Factor 1, Chorea, General Medicine, Endocrinology, Internal medicine, Pediatrics, Perinatology and Child Health, Brain-Lung-Thyroid Syndrome, Cancer research, medicine, Neurology (clinical), medicine.symptom, business, Novel mutation, Gene
تدمد: 1090-3798
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::59d48514e941069e3463ee0a094a4772Test
https://doi.org/10.1016/s1090-3798Test(13)70363-5
حقوق: CLOSED
رقم الانضمام: edsair.doi...........59d48514e941069e3463ee0a094a4772
قاعدة البيانات: OpenAIRE
الوصف
تدمد:10903798