GENETIC HETEROGENEITY OF ALPHA-GALACTOSIDASE IN FABRYS-DISEASE

被引：32

作者：

ROMEO, G

CHILDS, B

MIGEON, BR

机构：

来源：

FEBS LETTERS | 1972年 / 27卷 / 01期

关键词：

D O I：

10.1016/0014-5793(72)80432-0

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：161 / &

共 23 条

[1]

BEUTLER E, 1972, AM J HUM GENET, V24, P237

[2] ENZYMATIC DEFECT IN FABRYS DISEASE - CERAMIDETRIHEXOSIDASE DEFICIENCY [J].

BRADY, RO ;

GAL, AE ;

BRADLEY, RM ;

MARTENSS.E ;

WARSHAW, AL ;

LASTER, L .

NEW ENGLAND JOURNAL OF MEDICINE, 1967, 276 (21) :1163-&

[3] FABRYS DISEASE - ANTENATAL DETECTION [J].

BRADY, RO ;

UHLENDORF, BW ;

JACOBSON, CB .

SCIENCE, 1971, 172 (3979) :174-+

[4] CERAMIDE TRIHEXOSIDOSIS (FABRYS DISEASE) WITHOUT SKIN LESIONS [J].

CLARKE, JTR ;

KNAACK, J ;

CRAWHALL, JC ;

WOLFE, LS .

NEW ENGLAND JOURNAL OF MEDICINE, 1971, 284 (05) :233-&

[5]

CLARKE JTR, 1971, J BIOL CHEM, V246, P5563

[6]

DITTMER JC, 1964, J LIPID RES, V5, P126

[7]

GRZESCHICK KH, IN PRESS

[8]

HAKOMORI SI, 1971, J BIOL CHEM, V246, P2271

[9]

HANDA S, 1971, J BIOCHEM-TOKYO, V69, P625

[10]

HO MW, 1972, AM J HUM GENET, V24, P256

← 1 2 3 →