EIF2AK3, encoding translation initiation factor 2-α kinase 3, is mutated in patients with Wolcott-Rallison syndrome

Nature Genetics

Volumn 25, Issue 4, 2000, Pages 406-409

  Delépine, Marc ^a   Nicolino, Marc ^b   Barrett, Timothy ^c   Golamaully, Mahamadee ^a   Mark Lathrop, G ^a   Julier, Cécile ^d,e  

^a CENTRE NATIONAL DE GÉNOTYPAGE   (France)

^b HÔPITAL DEBROUSSE   (France)

^c BIRMINGHAM CHILDREN S HOSPITAL   (United Kingdom)

^d INSTITUT PASTEUR   (France)

^e UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; MICROSATELLITE DNA; PHOSPHOTRANSFERASE; PROTEIN EIF2AK3; PROTEIN SERINE THREONINE KINASE; TRANSLATION INITIATION FACTOR 2ALPHA KINASE 3; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 2P; CHROMOSOME MAP; CONSANGUINEOUS MARRIAGE; CONTROLLED STUDY; ENZYME ACTIVE SITE; EPIPHYSIS DISEASE; FEMALE; GENE MUTATION; GENETIC LINKAGE; GROWTH RETARDATION; HOMOZYGOSITY; HUMAN; INFANT; INSULIN DEPENDENT DIABETES MELLITUS; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE SEQUENCE; OSTEOPOROSIS; PRIORITY JOURNAL; TRANSLATION INITIATION; WOLCOTT RALLISON SYNDROME;

EUKARYOTA;

EID: 0034425698     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/78085     Document Type: Article

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