Creatine transporter defect diagnosed by proton NMR spectroscopy in males with intellectual disability

E-ISSN： 1552-4833|155|10|2446-2452

ISSN： 1552-4825

Source： American Journal Of Medical Genetics Part A, Vol.155, Iss.10, 2011-10, pp. : 2446-2452

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

Tau's role in the developing brain: implications for intellectual disability

By Sapir Tamar Frotscher Michael Levy Talia Mandelkow Eva-Maria Reiner Orly

Human Molecular Genetics, Vol. 21, Iss. 8, 2012-04 ,pp. : 1681-1692

Oxford University Press

Access to resources Recommend Favorite

Intellectual Disability and Cerebral Palsy in a UK Community

Public Health Genomics, Vol. 5, Iss. 3, 2002-11 ,pp. : 201-204

Karger

Access to resources Recommend Favorite

Identifying Genes Responsible for Intellectual Disability in Consanguineous Families

Human Heredity, Vol. 77, Iss. 1-4, 2014-07 ,pp. : 150-160

Karger

Access to resources Recommend Favorite

RBBP8 syndrome with microcephaly, intellectual disability, short stature and brachydactyly

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 12, 2015-12 ,pp. : 3148-3152

John Wiley & Sons Inc

Access to resources Recommend Favorite

Intellectual Disability in a Birth Cohort: Prevalence, Etiology, and Determinants at the Age of 4 Years

Public Health Genomics, Vol. 19, Iss. 5, 2016-09 ,pp. : 290-297

Karger

Access to resources Recommend Favorite