Truncating mutations in APP cause a distinct neurological phenotype

Publisher： John Wiley & Sons Inc

E-ISSN： 1531-8249|80|3|456-460

ISSN： 0364-5134

Source： ANNALS OF NEUROLOGY, Vol.80, Iss.3, 2016-09, pp. : 456-460

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

KIF5A mutations cause an infantile onset phenotype including severe myoclonus with evidence of mitochondrial dysfunction

By  

ANNALS OF NEUROLOGY, Vol. 80, Iss. 4, 2016-10 ,pp. : 633-637

John Wiley & Sons Inc

Access to resources Recommend Favorite

Truncating Mutations in the Chloride/Proton ClC-5 Antiporter Gene in Seven Jewish Israeli Families with Dent’s 1 Disease

By  

Nephron Clin Pract, Vol. 112, Iss. 4, 2009-06 ,pp. : c262-c267

Karger

Access to resources Recommend Favorite

Mutations in CIZ1 are not a major cause for dystonia in Germany

By  

MOVEMENT DISORDERS, Vol. 30, Iss. 5, 2015-04 ,pp. : 740-743

John Wiley & Sons Inc

Access to resources Recommend Favorite

Recessive ITPA mutations cause an early infantile encephalopathy

By  

ANNALS OF NEUROLOGY, Vol. 78, Iss. 4, 2015-10 ,pp. : 649-658

John Wiley & Sons Inc

Access to resources Recommend Favorite

Mutations in KCNT1 cause a spectrum of focal epilepsies

By  

EPILEPSIA, Vol. 56, Iss. 9, 2015-09 ,pp. : e114-e120

John Wiley & Sons Inc

Access to resources Recommend Favorite