التفاصيل البيبلوغرافية
| العنوان: |
Thyroid involvement in Chanarin-Dorfman syndrome in adults in the largest series of patients carrying the same founder mutation in ABHD5 gene |
| المؤلفون: |
Louhichi, Nacim, Bahloul, Emna, Marrakchi, Slaheddine, Othman, Houda Ben, Triki, Chahnez, Aloulou, Kawthar, Trabelsi, Lobna, Mahfouth, Nadia, Ayadi-Mnif, Zeineb, Keskes, Leila, Fakhfakh, Faiza, Turki, Hamida |
| المصدر: |
Orphanet Journal of Rare Diseases ; volume 14, issue 1 ; ISSN 1750-1172 |
| بيانات النشر: |
Springer Science and Business Media LLC |
| سنة النشر: |
2019 |
| مصطلحات موضوعية: |
Pharmacology (medical), Genetics (clinical), General Medicine |
| نوع الوثيقة: |
article in journal/newspaper |
| اللغة: |
English |
| DOI: |
10.1186/s13023-019-1095-4 |
| DOI: |
10.1186/s13023-019-1095-4.pdf |
| DOI: |
10.1186/s13023-019-1095-4/fulltext.html |
| الإتاحة: |
https://doi.org/10.1186/s13023-019-1095-4Test |
| حقوق: |
http://creativecommons.org/licenses/by/4.0Test/ ; http://creativecommons.org/licenses/by/4.0Test/ |
| رقم الانضمام: |
edsbas.8F2B5E9B |
| قاعدة البيانات: |
BASE |
