SCOPUS 정보 검색 플랫폼

Volumn 165, Issue 1, 2006, Pages 62-63

Limb girdle muscular dystrophy type 2I caused by a novel missense mutation in the FKRP gene presenting as acute virus-associated myositis in infancy

(7) Von Der Hagen, Maja Der a Kaindl, Angela M b Koehler, Kathrin c Mitzscherling, Petra c Häusler, Hans Jürgen c Stoltenburg Didinger, Gisela b Huebner, Angela c

a DRESDEN UNIVERSITY OF TECHNOLOGY (Germany)

b CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN (Germany)

c UNIVERSITY HOSPITAL CARL GUSTAV CARUS (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; FUKUTIN;

ADOLESCENT; ANAMNESIS; ARTICLE; CASE REPORT; CLINICAL FEATURE; CONGESTIVE CARDIOMYOPATHY; DIAGNOSTIC IMAGING; DIFFERENTIAL DIAGNOSIS; FUKUTIN RELATED PROTEIN GENE; GENE; GENETIC COUNSELING; HAPLOTYPE; HUMAN; LABORATORY TEST; LIMB GIRDLE MUSCULAR DYSTROPHY; MALE; MISSENSE MUTATION; MYOSITIS; PHYSICAL EXAMINATION; PRESCHOOL CHILD; PRIORITY JOURNAL;

CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; HUMANS; INFANT; LINKAGE (GENETICS); MALE; MUSCULAR DYSTROPHIES, LIMB-GIRDLE; MUTATION, MISSENSE; MYOSITIS; PHENOTYPE; PROTEINS;

EID: 29244468890 PISSN: 03406199 EISSN: None Source Type: Journal
DOI: 10.1007/s00431-005-1752-6 Document Type: Article

Times cited : (7)

References (6)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.