Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Marcos J, Aguiar"'
Autor:
Débora Marques de Miranda, Marcos J. Aguiar, Bruna Araújo Martins Resende, Cristina T Fonseca, Luiz De Marco, Daniela M Amaral, José Maria Correia Lima e Silva, Bernardo Léo Wajchenberg, Márcia Gonçalves Ribeiro, W. L. Boson, Maria Regina Calsolari
Publikováno v:
Clinical Endocrinology. 71:512-517
Summary Context Congenital generalized lipodystrophy, or Berardinelli–Seip syndrome, is a rare autosomal recessive disease caused by mutations in either the BSCL2 or AGPAT2 genes. This syndrome is characterized by an almost complete loss of adipose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15562db74c5c52b47019a6bc9c5a834b
https://doi.org/10.1111/j.1365-2265.2009.03532.x
https://doi.org/10.1111/j.1365-2265.2009.03532.x
Autor:
Debora M, Miranda, Bernardo L, Wajchenberg, Maria R, Calsolari, Marcos J, Aguiar, José M C L, Silva, Marcia G, Ribeiro, Cristina, Fonseca, Daniela, Amaral, Wolfanga L, Boson, Bruna A, Resende, Luiz, De Marco
Publikováno v:
Clinical endocrinology. 71(4)
Congenital generalized lipodystrophy, or Berardinelli-Seip syndrome, is a rare autosomal recessive disease caused by mutations in either the BSCL2 or AGPAT2 genes. This syndrome is characterized by an almost complete loss of adipose tissue usually di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e362b56436147a8744155c28a24f45a9
https://pubmed.ncbi.nlm.nih.gov/19226263
https://pubmed.ncbi.nlm.nih.gov/19226263