[Two novel EIF2AK3 mutations in a Chinese boy with Wolcott-Rallison syndrome].

Zhonghua er ke za zhi. Chinese journal of pediatrics

Volumn 49, Issue 4, 2011, Pages 301-305

  Feng, Dai Rong ^a   Meng, Yan ^b   Zhao, Shi Min ^b   Shi, Hui Ping ^b   Wang, Wei Chen ^b   Huang, Shang Zhi ^b  

^a INSTITUTE OF BASIC MEDICAL SCIENCES   (China)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

EIF2AK3 PROTEIN, HUMAN; PROTEIN KINASE R;

ARTICLE; CASE REPORT; CHILD; CHONDRODYSPLASIA; CONGENITAL MALFORMATION; EPIPHYSIS; GENETICS; HUMAN; INSULIN DEPENDENT DIABETES MELLITUS; MALE; MUTATION;

CHILD; DIABETES MELLITUS, TYPE 1; EIF-2 KINASE; EPIPHYSES; HUMANS; MALE; MUTATION; OSTEOCHONDRODYSPLASIAS;

EID: 80355145112     PISSN: 05781310     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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