A GENETICAL ANALYSIS OF 30 FAMILIES WITH WILSONS DISEASE - HEPATOLENTICULAR DEGENERATION

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BEARN, AG
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Q3 [遗传学];
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071007 ; 090102 ;
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页码:33 / 43
页数:11
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[1]  
BEARN A G, 1956, Postgrad Med J, V32, P477
[2]   ABNORMALITIES OF COPPER METABOLISM IN WILSONS DISEASE AND THEIR RELATIONSHIP TO THE AMINOACIDURIA [J].
BEARN, AG ;
KUNKEL, HG .
JOURNAL OF CLINICAL INVESTIGATION, 1954, 33 (03) :400-409
[3]   GENETIC AND BIOCHEMICAL ASPECTS OF WILSONS DISEASE [J].
BEARN, AG .
AMERICAN JOURNAL OF MEDICINE, 1953, 15 (04) :442-449
[5]  
BEARN AG, 1959, P ROY SOC MED, V52, P61
[6]  
BICKEL H, 1957, Q J MED, V26, P527
[7]   SEPARATION AND CHARACTERIZATION OF 2 COERULOPLASMINS FROM HUMAN SERUM [J].
BROMAN, L .
NATURE, 1958, 182 (4650) :1655-1657
[8]  
BROMAN L, 1959, UNPUB
[9]   STUDIES ON COPPER METABOLISM .13. HEPATOLENTICULAR DEGENERATION [J].
CARTWRIGHT, GE ;
HODGES, RE ;
GUBLER, CJ ;
MAHONEY, JP ;
DAUM, K ;
WINTROBE, MM ;
BEAN, WB .
JOURNAL OF CLINICAL INVESTIGATION, 1954, 33 (11) :1487-1501
[10]  
Compston A., 1912, BRAIN, V34, P295, DOI DOI 10.1093/BRAIN/34.4.295