Novel compound heterozygous mutations T2C and 1149insT in the KCNQ1 gene cause Jervell and Lange-Nielsen syndrome

Author：            

Publisher： Spandidos Publications

ISSN： 1107-3756

Source： International Journal of Molecular Medicine, Vol.28, Iss.1, 2011-01, pp. : 41-46

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

Novel compound heterozygous mutations in PRKRA cause pure dystonia

By  

MOVEMENT DISORDERS, Vol. 30, Iss. 6, 2015-05 ,pp. : 877-878

John Wiley & Sons Inc

Access to resources Recommend Favorite

Reply to letter: Novel compound heterozygous mutations in PRKRA cause pure dystonia

By  

MOVEMENT DISORDERS, Vol. 30, Iss. 6, 2015-05 ,pp. : 878-879

John Wiley & Sons Inc

Access to resources Recommend Favorite

Compound Heterozygous Mutations of the SBDS Gene in a Patient with Shwachman-Diamond Syndrome, Type 1 Diabetes Mellitus and Osteoporosis

By  

Pancreatology, Vol. 6, Iss. 6, 2007-03 ,pp. : 549-554

Karger

Access to resources Recommend Favorite

Autosomal Recessive von Willebrand Disease Type 1 or 2 due to Homozygous or Compound Heterozygous Mutations in the von Willebrand Factor Gene

By  

Acta Haematologica, Vol. 121, Iss. 2-3, 2009-06 ,pp. : 106-110

Karger

Access to resources Recommend Favorite

T-Helper 1, T-Helper 2, and T-Regulatory Cytokines Gene Polymorphisms in Irritable Bowel Syndrome

By Barkhordari Elham   Rezaei Nima   Mahmoudi Mahdi   Larki Pegah   Ahmadi-Ashtiani Hamid   Ansaripour Bita   Alighardashi Maryam   Bashashati Mohammad   Amirzargar Ali   Ebrahimi-Daryani Naser  

Inflammation, Vol. 33, Iss. 5, 2010-10 ,pp. : 281-286

Springer Publishing Company

Access to resources Recommend Favorite