Clinical and Genetic Analysis of a Korean Patient with Late-onset X-linked Adrenal Hypoplasia Congenita and Hypogonadotropic Hypogonadism: Identification of a Novel Mutation in the NR0B1 Gene

Author： Lee Y-W   Won JC   Ki C-S   Lee HY   Ahn HS   Lee YK   Kim YH   Kim C-H  

Publisher： Field House Publishing

ISSN： 0300-0605

Source： The Journal of International Medical Research, Vol.36, Iss.2, 2008-03, pp. : 357-361

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Molecular Analysis of a Novel Cathepsin K Gene Mutation in a Chinese Child with Pycnodysostosis

By Li H-Y   Ma H-W   Wang H-Q   Ma W-H  

The Journal of International Medical Research, Vol. 37, Iss. 1, 2009-01 ,pp. : 264-269

Field House Publishing

Access to resources Recommend Favorite

Genetic polymorphisms of CYP1A1 in a Korean population

By Park Duk  

Archives of Toxicology, Vol. 78, Iss. 6, 2004-06 ,pp. : 306-308

Springer Publishing Company

Access to resources Recommend Favorite

Preimplantation genetic diagnosis of X-linked retinoschisis

By Lledó Belén   Ten Jorge   Rodriguez-Arnedo Dori   Llácer Joaquín   Bernabeu Rafael  

Reproductive BioMedicine Online, Vol. 16, Iss. 6, 2008-06 ,pp. : 886-892

Reproductive Healthcare Ltd

Access to resources Recommend Favorite

Potential Application of Gene Therapy to X-Linked Agammaglobulinemia

By  

Current Gene Therapy, Vol. 7, Iss. 4, 2007-08 ,pp. : 284-294

Bentham Science Publishers

Access to resources Recommend Favorite

Identification of a Novel de novo STK11 Mutation in a Chinese Child with Peutz–Jeghers Syndrome

By Liu W-L   Li F   He Z-X   Jiang H-Y   Ai R   Zhu X-P   Chen X-X   Ma H-W  

The Journal of International Medical Research, Vol. 39, Iss. 5, 2011-09 ,pp. : 2033-2038

Field House Publishing

Access to resources Recommend Favorite