TY  - GEN
AU  - Gong,Chun-xiu
AU  - Wen,Ya-ran
AU  - Zhao,Xiu-li
AU  - Su,Chang
AU  - Cao,Bing-yan
AU  - Zhang,Xue
TI  - [Allgrove syndrome in the mainland of China: clinical report and mutation analysis]
SN  - 0578-1310
PY  - 2010///1029
KW  - Adrenal Insufficiency
KW  - genetics
KW  - Adrenocorticotropic Hormone
KW  - blood
KW  - China
KW  - Consanguinity
KW  - DNA
KW  - analysis
KW  - DNA Mutational Analysis
KW  - Esophageal Achalasia
KW  - Exons
KW  - Female
KW  - Genetic Diseases, Inborn
KW  - Humans
KW  - Lacrimal Apparatus Diseases
KW  - Mutation
KW  - Nerve Tissue Proteins
KW  - Nuclear Pore Complex Proteins
KW  - Optic Atrophy
N1  - Publication Type: English Abstract; Journal Article
ER  -