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Volumn 44, Issue 1, 1998, Pages 140-143

Genetic characteristics of myoadenylate deaminase deficiency

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE MONOPHOSPHATE DEAMINASE;

EID: 0031926570     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410440124     Document Type: Article
Times cited : (64)

References (16)
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  • 3
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  • 4
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    • Molecular analysis of the myoadenylate deaminase deficiencies
    • Sabina RL, Fishbein WN, Pezeshkpour G, et al. Molecular analysis of the myoadenylate deaminase deficiencies. Neurology 1992;42:170-179
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    • Sabina, R.L.1    Fishbein, W.N.2    Pezeshkpour, G.3
  • 5
    • 0018772955 scopus 로고
    • Myoadenylate deaminase deficiency
    • Shumate JB, Katnik R, Ruiz M, et al. Myoadenylate deaminase deficiency. Muscle Nerve 1979;2:213-216
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    • Shumate, J.B.1    Katnik, R.2    Ruiz, M.3
  • 6
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    • Myoadenylate deaminase deficiency: A clinical and biochemical study in nine families
    • Sinkeler SPT, Joosten EMG, Wevers RA, et al. Myoadenylate deaminase deficiency: a clinical and biochemical study in nine families. Muscle Nerve 1988;11:312-317
    • (1988) Muscle Nerve , vol.11 , pp. 312-317
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  • 7
    • 0020047975 scopus 로고
    • Familial MAD deficiency and exertional myalgia
    • Kelemen J, Rice DR, Bradley WG, et al. Familial MAD deficiency and exertional myalgia. Neurology 1982;32:857-863
    • (1982) Neurology , vol.32 , pp. 857-863
    • Kelemen, J.1    Rice, D.R.2    Bradley, W.G.3
  • 8
    • 15444357446 scopus 로고
    • Immunologic uniqueness of muscle adenylate deaminase and genetic transmission of the deficiency state
    • Abstract
    • Fishbein WN, Griffin JL, Nagarayan K, et al. Immunologic uniqueness of muscle adenylate deaminase and genetic transmission of the deficiency state. Clin Res 1979;27:274A (Abstract)
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    • Fishbein, W.N.1    Griffin, J.L.2    Nagarayan, K.3
  • 10
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  • 12
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  • 13
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    • Double trouble: Combined myophosphorylase and AMP deaminase deficiency in a child homozygous for nonsense mutations at both loci
    • Tsujino S, Shanske S, Carroll JE, et al. Double trouble: combined myophosphorylase and AMP deaminase deficiency in a child homozygous for nonsense mutations at both loci. Neuromusc Disord 1995;5:263-266
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  • 14
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  • 15
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.