[Allgrove syndrome in the mainland of China: clinical report and mutation analysis].

Zhonghua er ke za zhi. Chinese journal of pediatrics

Volumn 45, Issue 6, 2007, Pages 422-425

  Gong, Chun xiu ^a   Wen, Ya ran ^b   Zhao, Xiu li ^b   Su, Chang ^b   Cao, Bing yan ^b   Zhang, Xue ^b  

^a CAPITAL MEDICAL UNIVERSITY   (China)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

AAAS PROTEIN, HUMAN; CORTICOTROPIN; DNA; NERVE PROTEIN; NUCLEOPORIN;

ADRENAL INSUFFICIENCY; ARTICLE; BLOOD; CHINA; CONSANGUINITY; ESOPHAGUS ACHALASIA; EXON; FEMALE; GENETIC DISORDER; GENETICS; HUMAN; LACRIMAL GLAND DISEASE; MUTATION; NUCLEOTIDE SEQUENCE; OPTIC NERVE ATROPHY; PATHOPHYSIOLOGY;

ADRENAL INSUFFICIENCY; ADRENOCORTICOTROPIC HORMONE; CHINA; CONSANGUINITY; DNA; DNA MUTATIONAL ANALYSIS; ESOPHAGEAL ACHALASIA; EXONS; FEMALE; GENETIC DISEASES, INBORN; HUMANS; LACRIMAL APPARATUS DISEASES; MUTATION; NERVE TISSUE PROTEINS; NUCLEAR PORE COMPLEX PROTEINS; OPTIC ATROPHY;

EID: 79958296185     PISSN: 05781310     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)