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Volumn 335, Issue 1-2, 2003, Pages 21-26

A simple, rapid test for the differential diagnosis of glycogen storage disease type 3

Author keywords

Creatine kinase; Debrancher deficiency

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CARDIOMYOPATHY; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; DIFFERENTIAL DIAGNOSIS; EVALUATION; FEMALE; GLYCOGEN STORAGE DISEASE TYPE 3; HEPATOSPLENOMEGALY; HUMAN; MALE; METABOLIC DISORDER; MYOPATHY; PRIORITY JOURNAL;

EID: 0242380330     PISSN: 00098981     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0009-8981(03)00234-1     Document Type: Article
Times cited : (9)

References (8)
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  • 2
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  • 4
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    • Lack of an alpha-1,4 glucan: 1,4 glucan 6-glucoyle tranferase in a case of type 4 glycogenosis
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    • [Suppl.]
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  • 6
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    • Molecular cloning and nucleotide sequence of cDNA encoding human muscle debranching enzyme
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    • Genotype-phenotype correlation in two frequent mutations and mutation update in type III glycogen storage disease
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.