Recurrent drop attacks in early childhood as presenting symptom of benign hereditary chorea caused by TITF1 gene mutations

Publisher： John Wiley & Sons Inc

E-ISSN： 1469-8749|57|8|777-779

ISSN： 0012-1622

Source： DEVELOPMENTAL MEDICINE & CHILD NEUROLOGY, Vol.57, Iss.8, 2015-08, pp. : 777-779

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 and Recurrent Mutations in the C1NH Gene of Arab Patients Affected with Hereditary Angioedema

By  

International Archives of Allergy and Immunology, Vol. 151, Iss. 2, 2009-09 ,pp. : 149-154

Karger

Access to resources Recommend Favorite

Hereditary Hyperekplexia caused by Novel Mutations of GLRA1 in Turkish Families

By Gilbert Sandra L.  

Molecular Diagnosis, Vol. 8, Iss. 3, 2004-01 ,pp. : 151-155

Adis International

Access to resources Recommend Favorite

ADCY5 identified as a novel cause of benign hereditary chorea

By  

MOVEMENT DISORDERS, Vol. 30, Iss. 13, 2015-11 ,pp. : 1726-1726

John Wiley & Sons Inc

Access to resources Recommend Favorite

Hereditary hypochromic microcytic anemia associated with loss‐of‐function DMT1 gene mutations and absence of liver iron overload

By  

AMERICAN JOURNAL OF HEMATOLOGY, Vol. 93, Iss. 3, 2018-03 ,pp. : E58-E60

John Wiley & Sons Inc

Access to resources Recommend Favorite

Hereditary angioedema with normal C1‐INH with versus without specific F12 gene mutations

By  

ALLERGY, Vol. 70, Iss. 8, 2015-08 ,pp. : 1004-1012

John Wiley & Sons Inc

Access to resources Recommend Favorite