Mutations in HTRA2 are not a common cause of familial classic ET

Publisher： John Wiley & Sons Inc

E-ISSN： 1531-8257|30|8|1149-1150

ISSN： 0885-3185

Source： MOVEMENT DISORDERS, Vol.30, Iss.8, 2015-07, pp. : 1149-1150

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

DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy

By  

EPILEPSIA, Vol. 13-9580, Iss. 10, 2015-10 ,pp. : e168-e171

John Wiley & Sons Inc

Access to resources Recommend Favorite

DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy

By  

EPILEPSIA, Vol. 56, Iss. 10, 2015-10 ,pp. : e168-e171

John Wiley & Sons Inc

Access to resources Recommend Favorite

Mutations in the cardiac myosin-binding protein C gene are the predominant cause of familial hypertrophic cardiomyopathy in eastern Finland

By Jääskeläinen Pertti   Kuusisto Johanna   Miettinen Raija   Kärkkäinen Päivi   Kärkkäinen Satu   Heikkinen Sami   Peltola Paula   Pihlajamäki Jussi   Vauhkonen Ilkka   Laakso Markku  

Journal of Molecular Medicine, Vol. 80, Iss. 7, 2002-07 ,pp. : 412-422

Springer Publishing Company

Access to resources Recommend Favorite

DYT2 revealed: Hippocalcin mutations cause autosomal‐recessive isolated dystonia

By  

MOVEMENT DISORDERS, Vol. 30, Iss. 13, 2015-11 ,pp. : 1725-1725

John Wiley & Sons Inc

Access to resources Recommend Favorite

CHCHD10 mutations are not a common cause of SMN1‐negative type III/IV spinal motor atrophy

By  

ANNALS OF NEUROLOGY, Vol. 78, Iss. 5, 2015-11 ,pp. : 831-831

John Wiley & Sons Inc

Access to resources Recommend Favorite