Contiguous deletion of SLC6A8 and BAP31 in a patient with severe dystonia and sensorineural deafness-Reference-Cited by-同舟云学术

Contiguous deletion of SLC6A8 and BAP31 in a patient with severe dystonia and sensorineural deafness

Published:2012-05 Issue:1 Volume:106 Page:43-47
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Osaka Hitoshi,Takagi Atsushi,Tsuyusaki Yu,Wada Takahito,Iai Mizue,Yamashita Sumimasa,Shimbo Hiroko,Saitsu Hirotomo,Salomons Gajja S.,Jakobs Cornelis,Aida Noriko,Toshihiro Shinka,Kuhara Tomiko,Matsumoto Naomichi

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference20 articles.

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5. Incidence of brain creatine transporter deficiency in males with developmental delay referred for brain magnetic resonance imaging;Newmeyer;J. Dev. Behav. Pediatr.,2005

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