A novelPCLN-1gene mutation in familial hypomagnesemia with hypercalciuria and atypical phenotype

• 作者Sami A. Sanjad; Ali Hariri; Zouhayr M. Habbal; Richard P. Lifton
• 卷第22卷
• 期第4期
• 印刷ISSN0931-041X
• 电子ISSN1432-198X
• 文件大小183.42KB
• 发表时间2007-04
• DOI10.1007/s00467-006-0354-5
• 页码503-508