BIOCHEMICAL AND GENETIC STUDIES IN 2 FAMILIES WITH FABRY DISEASE

被引：11

作者：

GOTO, I

TABIRA, T

NAWA, A

KUROKAWA, T

KUROIWA, Y

机构：

[1] KYUSHU UNIV,FAC MED,DEPT PEDIAT,FUKUOKA,JAPAN

[2] KYUSHU UNIV,FAC MED,NEUROL INST,DEPT NEUROL,HIGASHI 812,FUKUOKA CITY,JAPAN

来源：

关键词：

D O I：

10.1001/archneur.1974.00490370071011

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：45 / 50

页数：6

共 26 条

[1] BEUTLER E, 1972, AM J HUM GENET, V24, P237
[2] BEUTLER E, 1972, J BIOL CHEM, V247, P7195
[3] ENZYMATIC DEFECT IN FABRYS DISEASE - CERAMIDETRIHEXOSIDASE DEFICIENCY
BRADY, RO
GAL, AE
BRADLEY, RM
MARTENSS.E
WARSHAW, AL
LASTER, L
[J]. NEW ENGLAND JOURNAL OF MEDICINE, 1967, 276 (21) : 1163 - &
[4] PETECHIAL ANGIOMATA
BRANNEN, M
NIXON, RK
FOSNAUGH, RP
DOUCETTE, JW
[J]. ARCHIVES OF DERMATOLOGY, 1961, 83 (03) : 386 - &
[5] ANGIOKERATOMA CORPORIS DIFFUSUM UNIVERSALE (FABRYS DISEASE) IN FEMALE SUBJECTS
BURDA, CD
WINDER, PR
[J]. AMERICAN JOURNAL OF MEDICINE, 1967, 42 (02) : 293 - &
[6] CERAMIDE TRIHEXOSIDOSIS (FABRYS DISEASE) WITHOUT SKIN LESIONS
CLARKE, JTR
KNAACK, J
CRAWHALL, JC
WOLFE, LS
[J]. NEW ENGLAND JOURNAL OF MEDICINE, 1971, 284 (05) : 233 - &
[7] GEMMINGEN GV, 1965, ARCH DERMATOL, V91, P206
[8] HANDA S, 1971, J BIOCHEM-TOKYO, V69, P625
[9] HO MW, 1972, AM J HUM GENET, V24, P256
[10] GENETIC ASPECTS OF ANGIOKERATOMA CORPORIS DIFFUSUM
JOHNSTON, AW
WARLAND, BJ
WELLER, SDV
[J]. ANNALS OF HUMAN GENETICS, 1966, 30 : 25 - &