Author response: Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression

التفاصيل البيبلوغرافية
العنوان: Author response: Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression
المؤلفون: Rocha, Nuno, Bulger, David A, Frontini, Andrea, Titheradge, Hannah, Gribsholt, Sigrid Bjerge, Knox, Rachel, Page, Matthew, Harris, Julie, Payne, Felicity, Adams, Claire, Sleigh, Alison, Crawford, John, Gjesing, Anette Prior, Bork-Jensen, Jette, Pedersen, Oluf, Barroso, Inês, Hansen, Torben, Cox, Helen, Reilly, Mary, Rossor, Alex, Brown, Rebecca J, Taylor, Simeon I, McHale, Duncan, Armstrong, Martin, Oral, Elif A, Saudek, Vladimir, O’Rahilly, Stephen, Maher, Eamonn R, Richelsen, Bjørn, Savage, David B, Semple, Robert K
بيانات النشر: eLife Sciences Publications, Ltd
سنة النشر: 2017
المجموعة: eLife (E-Journal - via CrossRef)
نوع الوثيقة: other/unknown material
اللغة: unknown
DOI: 10.7554/elife.23813.036
الإتاحة: https://doi.org/10.7554/elife.23813.036Test
حقوق: http://creativecommons.org/publicdomain/zero/1.0Test/
رقم الانضمام: edsbas.68FCDC31
قاعدة البيانات: BASE