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Volumn 53, Issue 10, 2004, Pages 2719-2722

Kir6.2 mutations are a common cause of permanent neonatal diabetes in a large cohort of French patients

(9) Vaxillaire, Martine a Populaire, Céline a Busiah, Kanetee b Cavé, Hélène c Gloyn, Anna L d Hattersley, Andrew T d Czernichow, Paul c Froguel, Philippe a,e Polak, Michel b

a INSTITUT PASTEUR DE LILLE (France)

b HÔPITAL NECKER ENFANTS MALADES (France)

c HÔPITAL ROBERT DEBRÉ (France)

d PENINSULA MEDICAL SCHOOL (United Kingdom)

e HAMMERSMITH HOSPITAL (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

INWARDLY RECTIFYING POTASSIUM CHANNEL SUBUNIT KIR6.2;

AMINO ACID SUBSTITUTION; ARTICLE; CLINICAL ARTICLE; COHORT ANALYSIS; DIABETES MELLITUS; FEMALE; FRANCE; GENE; GENE MUTATION; HUMAN; KCNJ11 GENE; MALE; MUTATION RATE; NEWBORN; PERMANENT NEONATAL DIABETES; PRIORITY JOURNAL;

BIRTH WEIGHT; DIABETES MELLITUS; EXONS; FEMALE; FRANCE; HUMANS; INFANT, NEWBORN; MALE; POTASSIUM CHANNELS, INWARDLY RECTIFYING; PROTEIN SUBUNITS;

EID: 4644309915 PISSN: 00121797 EISSN: None Source Type: Journal
DOI: 10.2337/diabetes.53.10.2719 Document Type: Article

Times cited : (173)

References (8)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.