[Allgrove syndrome in the mainland of China: clinical report and mutation analysis]. [electronic resource]
Producer: 20101029Description: 422-5 p. digitalISSN:- 0578-1310
- Adrenal Insufficiency -- genetics
- Adrenocorticotropic Hormone -- blood
- China
- Consanguinity
- DNA -- analysis
- DNA Mutational Analysis
- Esophageal Achalasia -- genetics
- Exons
- Female
- Genetic Diseases, Inborn -- genetics
- Humans
- Lacrimal Apparatus Diseases -- genetics
- Mutation
- Nerve Tissue Proteins -- genetics
- Nuclear Pore Complex Proteins -- genetics
- Optic Atrophy -- genetics
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Publication Type: English Abstract; Journal Article
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