Aspartylglucosaminuria in a Puerto Rican family: Additional features of a panethnic disorder

Author:

Chitayat David,Nakagawa Sachiko,Marion Robert W.,Sachs Gay S,Hahm Sue Y. E.,Goldman Harold S.,Opitz John M.,Reynolds James F.

Publisher

Wiley

Subject

Genetics (clinical)

Cited by 16 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Aspartylglucosaminuria: Clinical Presentation and Potential Therapies;Journal of Child Neurology;2021-01-13

2. Aspartylglucosaminuria;Journal of Child Neurology;2012-12-26

3. Two Japanese cases with aspartylglycosaminuria: clinical and morphological features;Clinical Genetics;2008-06-28

4. A;Taybi and Lachman's Radiology of Syndromes, Metabolic Disorders and Skeletal Dysplasias;2007

5. In Vivo FSH Actions;Sertoli Cell Biology;2005

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