Haploinsufficiency at GCK gene is not a frequent event in MODY2 patients

Clinical Endocrinology

Volumn 68, Issue 6, 2008, Pages 873-878

  Garin, Intza ^a   Rica, Itxaso ^a   Estalella, Itziar ^a   Oyarzabal, Mirentxu ^b   Rodríguez Rigual, Mercedes ^c   Pedro, Jose Ignacio San ^a   Pérez Nanclares, Gustavo ^a   Fernández Rebollo, Eduardo ^a   Busturia, Maria Angeles ^a   Castaño, Luis ^a   De Nanclares, Guiomar Pérez ^a   Abellan M ^d   Espiga J , ^d   Boronat, M ^d   Galicia, I ^d   Lamas, ^d   Lopez Capape M ^d   Unanue, G ^d   Fernandez C ^d   Sobradillo, B ^d   Rivas, F ^d   Leiva, I ^d   Prieto, J ^d   Lopez M J ^d   Hermoso, F ^d   Bueno, G ^e   Tapia, L ^d   Cortazar, A ^d   Gaztambide, S ^d   Martul, P ^d   Quintana, B ^d   Santamarea J ^d   Vazquez F ^d   Vela, A ^d   Aleixandre, F ^f   Reig, C ^d   Borras V ^d   Santos, L ^d   Calvo, T ^d   Rodreguez Rigual M ^d   Casas, J ^g   Gomez Vida J ^d   Forga, L ^d   Menendez E ^d   Rodréguez, Rial ^d   Luengo, J L ^d   Alonso, M ^d   Barrio, R ^d   Gastaldo, E ^d   Blasco, L ^d   Robira, A ^d   Garcia Cuartero, B ^d   Bel, J ^d   Anton A ^h   Diez, I ^h   Rodriguez, A ^h   Ruiz Cano, R ^d   Jimenez Bustos J M ^d   Fernandez, Ramirez ⁱ   Hernando, C ^d   Cedeno J ^j   Barreiro, J ^k   Luzuriaga, C ^d   Diaz De Grenu C ^d   Espino, R ^l   Oyarzabal, M ^d   Gomez Gila A ^m   more..

^a HOSPITAL DE CRUCES   (Spain)

^b Universidad Pública de Navarra   (Spain)

^c HOSPITAL UNIVERSITARIO MIGUEL SERVET   (Spain)

^d Complejo Hospitalario Donostia San Sebastian ^*

^e H Clénico Universitario Zaragoza

^f Hospital General Elda Alicante

^g HOSPITAL DE MÓSTOLES   (Spain)

^h HOSPITAL TXAGORRITXU   (Spain)

ⁱ HOSPITAL UNIVERSITARIO PRÍNCIPE DE ASTURIAS   (Spain)

^j Hospital Clnico Universitario de Salamanca   (Spain)

^k Instituto de Salud Carlos III

^l HOSPITAL UNIVERSITARIO DE VALME   (Spain)

^m HOSPITAL UNIVERSITARIO VIRGEN DEL ROCÍO   (Spain)

more..

Author keywords

[No Author keywords available]

Indexed keywords

GLUCOKINASE;

ADOLESCENT; ADULT; ARTICLE; BIRTH WEIGHT; CHILD; FEMALE; GCK GENE; GENE; GENE DELETION; GENE DOSAGE; GENE INSERTION; GENE MUTATION; GENOTYPE; GENOTYPE PHENOTYPE CORRELATION; GLUCOSE BLOOD LEVEL; HAPLOINSUFFICIENCY; HUMAN; INFANT; INTRAUTERINE GROWTH RETARDATION; LOW BIRTH WEIGHT; MAJOR CLINICAL STUDY; MALE; MATURITY ONSET DIABETES MELLITUS; PHENOTYPE; POINT MUTATION; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SPAIN;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; DIABETES MELLITUS, TYPE 2; FEMALE; GENE EXPRESSION REGULATION, ENZYMOLOGIC; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; MALE; MUTATION; PHENOTYPE; PROTEIN-SERINE-THREONINE KINASES; SPAIN;

EID: 43949103781     PISSN: 03000664     EISSN: 13652265     Source Type: Journal    
DOI: 10.1111/j.1365-2265.2008.03214.x     Document Type: Article

References (26)