Group by:
Date |
Item TypeArticle
HDAC4 mutations cause diabetes and induce β-cell FoxO1 nuclear exclusion.
Gong, M.
ORCID: https://orcid.org/0000-0001-7384-3429, Yu, Y.
ORCID: https://orcid.org/0000-0003-1928-2514, Liang, L., Vuralli, D., Froehler, S.
ORCID: https://orcid.org/0000-0001-8000-2927, Kuehnen, P., Du Bois, P., Zhang, J., Cao, A., Liu, Y., Hussain, K., Fielitz, J.
ORCID: https://orcid.org/0000-0001-8522-1045, Jia, S.
ORCID: https://orcid.org/0000-0001-8595-9314, Chen, W.
ORCID: https://orcid.org/0000-0003-3263-1627 and Raile, K.
ORCID: https://orcid.org/0000-0002-0842-1737
Molecular Genetics & Genomic Medicine 7
(5): e602.
May 2019
Unknown mutations and genotype/phenotype correlations of autosomal recessive congenital ichthyosis in patients from Saudi Arabia and Pakistan.
Lima Cunha, D.
ORCID: https://orcid.org/0000-0002-6814-8365, Alakloby, O.M., Gruber, R., Kakar, N., Ahmad, J., Alawbathani, S., Plank, R., Eckl, K.
ORCID: https://orcid.org/0000-0001-8838-3998, Krabichler, B., Altmüller, J.
ORCID: https://orcid.org/0000-0003-4372-1521, Nürnberg, P., Zschocke, J., Borck, G., Schmuth, M., Alabdulkareem, A.S., Abdulaziz Alnutaifi, K. and Hennies, H.C.
ORCID: https://orcid.org/0000-0001-7210-2389
Molecular Genetics & Genomic Medicine 7
(3): e539.
March 2019
Novel compound heterozygous mutations in TELO2 in a patient with severe expression of You-Hoover-Fong syndrome.
Moosa, S.
ORCID: https://orcid.org/0000-0002-4463-3067, Altmüller, J.
ORCID: https://orcid.org/0000-0003-4372-1521, Lyngbye, T., Christensen, R., Li, Y., Nürnberg, P., Yigit, G., Vogel, I.
ORCID: https://orcid.org/0000-0002-1125-0393 and Wollnik, B.
Molecular Genetics & Genomic Medicine 5
(5): 580-584.
September 2017
This list was generated on Wed Jun 17 23:07:59 2026 UTC.