Author: Baumgartner Matthias R.
Publisher: Oxford University Press
E-ISSN: 0964-6906|9|19|2853-2858
ISSN: 1460-2083
Source: Human Molecular Genetics, Vol.9, Iss.19, 2000-11, pp. : 2853-2858
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Related content
Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F 1 subunit
By Mayr Johannes A. Havlkov Vendula Zimmermann Franz Magler Iris Kaplanov Vilma Jeina Pavel Pecinov Alena Nskov Hana Koch Johannes Sperl Wolfgang Houtk Josef
Human Molecular Genetics, Vol. 19, Iss. 17, 2010-09 ,pp. :
By Muchir Antoine Shan Jian Bonne Gisle Lehnart Stephan E. Worman Howard J.
Human Molecular Genetics, Vol. 18, Iss. 2, 2009-01 ,pp. :
Familial Tetralogy of Fallot caused by mutation in the jagged1 gene
By Eldadah Z.A.
Human Molecular Genetics, Vol. 10, Iss. 2, 2001-01 ,pp. :
Hydrolethalus syndrome is caused by a missense mutation in a novel gene HYLS1
By Mee Lisa
Human Molecular Genetics, Vol. 14, Iss. 11, 2005-06 ,pp. :