Receptor expression-enhancing protein 1 gene (SPG31) mutations are rare in Chinese Han patients with hereditary spastic paraplegia

Autor:	Juan, Du, Lu, Shen, Guo-hua, Zhao, Yin-guang, Wang, Shu-sheng, Liao, Chong, Chen, Zhi-fan, Zhou, Ying-ying, Luo, Hong, Jiang, Kun, Xia, Bei-sha, Tang
Rok vydání:	2009
Předmět:	Adult Male Adolescent Spastic Paraplegia Hereditary Infant Membrane Transport Proteins Sequence Analysis DNA Middle Aged Polymerase Chain Reaction Young Adult Asian People Child Preschool Mutation Humans Female Child
Zdroj:	Chinese medical journal. 122(17)
ISSN:	2542-5641
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid________::68ef084979dfe17caccaea6686243f71 https://pubmed.ncbi.nlm.nih.gov/19781397 Zobrazit plný text záznamu