X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy

Nature Genetics

Volumn 27, Issue 1, 2001, Pages 18-20

  Wildin, Robert S ^a   Ramsdell, Fred ^b   Peake, Jane ^c   Faravelli, Francesca ^d   Casanova, Jean Laurent ^e   Buist, Neil ^a   Levy Lahad, Ephrat ^f   Mazzella, Massimo ^g   Goulet, Olivier ^e   Perroni, Lucia ^d   Dagna Bricarelli, Franca ^d   Byrne, Geoffrey ^h   McEuen, Mark ^b   Proll, Sean ^b   Appleby, Mark ^b   Brunkow, Mary E ^b  

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^b Celltech Chiroscience Inc   (United States)

^c ROYAL CHILDREN'S HOSPITAL   (Australia)

^d GALLIERA HOSPITAL   (Italy)

^e HÔPITAL NECKER ENFANTS MALADES   (France)

^f SHAARE ZEDEK MEDICAL CENTER   (Israel)

^g G GASLINI INSTITUTE   (Italy)

^h PRINCESS MARGARET HOSPITAL FOR CHILDREN   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA;

ARTICLE; DIABETES MELLITUS; ENDOCRINE DISEASE; ENTEROPATHY; GENE MUTATION; GENOME; HUMAN; MAJOR CLINICAL STUDY; NEWBORN DISEASE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; THROMBOCYTOPENIA; X CHROMOSOME LINKAGE; X CHROMOSOME LINKED DISORDER; X CHROMOSOME RECESSIVE DISORDER;

AMINO ACID SEQUENCE; ANIMAL DISEASES; ANIMALS; DIABETES MELLITUS; DISEASE MODELS, ANIMAL; DNA MUTATIONAL ANALYSIS; DNA-BINDING PROTEINS; FORKHEAD TRANSCRIPTION FACTORS; HUMANS; INFANT, NEWBORN; LINKAGE (GENETICS); MICE; MICE, MUTANT STRAINS; MOLECULAR SEQUENCE DATA; MUTATION; POLYENDOCRINOPATHIES, AUTOIMMUNE; PROTEIN-LOSING ENTEROPATHIES; SEQUENCE ALIGNMENT; SYNDROME; X CHROMOSOME;

EID: 0035163909     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/83707     Document Type: Article

References (13)