Academic Journal

Monogenic forms of childhood obesity due to mutations in the leptin gene

التفاصيل البيبلوغرافية
العنوان: Monogenic forms of childhood obesity due to mutations in the leptin gene
المؤلفون: Funcke, Jan-Bernd, von Schnurbein, Julia, Lennerz, Belinda, Lahr, Georgia, Debatin, Klaus-Michael, Fischer-Posovszky, Pamela, Wabitsch, Martin
المصدر: Molecular and Cellular Pediatrics ; volume 1, issue 1 ; ISSN 2194-7791
بيانات النشر: Springer Science and Business Media LLC
سنة النشر: 2014
الوصف: Congenital leptin deficiency is a rare autosomal recessive monogenic obesity syndrome caused by mutations in the leptin gene. This review describes the molecular and cellular characteristics of the eight distinct mutations found so far in humans.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1186/s40348-014-0003-1
DOI: 10.1186/s40348-014-0003-1.pdf
DOI: 10.1186/s40348-014-0003-1/fulltext.html
الاتاحة: http://dx.doi.org/10.1186/s40348-014-0003-1
http://link.springer.com/content/pdf/10.1186/s40348-014-0003-1.pdf
http://link.springer.com/article/10.1186/s40348-014-0003-1/fulltext.html
http://link.springer.com/content/pdf/10.1186/s40348-014-0003-1
https://link.springer.com/content/pdf/10.1186/s40348-014-0003-1.pdf
Rights: http://creativecommons.org/licenses/by/4.0
رقم الانضمام: edsbas.10AFB63F
قاعدة البيانات: BASE
الوصف
DOI:10.1186/s40348-014-0003-1