Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Rare Diseases

Last data update: Nov 3, 2024. (Total: 233167Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 2 (of 2 Records)

Query Trace: Multiple Carboxylase Deficiency[original query]
Holocarboxylase synthetase deficiency: novel clinical and molecular findings.
Clinical genetics 2010 1 78 (1): 88-93.
Tammachote R, Janklat S, Tongkobpetch S, Suphapeetiporn K, Shotelersuk
Case report of holocarboxylase synthetase deficiency (late-onset) in 2 Chinese patients.
Medicine 2020 5 99 (18): e19964.
Xiong Zihong, Zhang Guoying, Luo Xiaoli, Zhang Ning, Zheng Ji
TOP