HEXOSAMINIDASE A DEFICIENT ADULTS - PRESENCE OF ALPHA-CHAIN PRECURSOR IN CULTURED SKIN FIBROBLASTS

被引:15
作者
FRISCH, A
BARAM, D
NAVON, R
机构
[1] TEL AVIV UNIV,SACKLER FAC MED,DEPT HUMAN GENET,TEL HASHOMER,ISRAEL
[2] CHAIM SHEBA MED CTR,IL-52621 TEL HASHOMER,ISRAEL
关键词
D O I
10.1016/0006-291X(84)91624-3
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
收藏
页码:101 / 107
页数:7
相关论文
共 9 条
  • [1] ARGOV Z, 1983, UNPUB
  • [2] HASILIK A, 1980, J BIOL CHEM, V255, P4937
  • [3] NAVON R, 1976, AM J HUM GENET, V28, P339
  • [4] NAVON R, 1973, AM J HUM GENET, V25, P287
  • [5] OBRIEN JS, 1983, METABOLIC BASIS INHE, P945
  • [6] PADEH B, 1971, ISRAEL J MED SCI, V7, P259
  • [7] SYNTHESIS OF BETA-HEXOSAMINIDASE IN CELL-FREE TRANSLATION AND IN INTACT FIBROBLASTS - AN INSOLUBLE PRECURSOR ALPHA-CHAIN IN A RARE FORM OF TAY-SACHS DISEASE
    PROIA, RL
    NEUFELD, EF
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (20): : 6360 - 6364
  • [8] ADULT (CHRONIC) GM2 GANGLIOSIDOSIS - ATYPICAL SPINOCEREBELLAR DEGENERATION IN A JEWISH SIBSHIP
    RAPIN, I
    SUZUKI, K
    SUZUKI, K
    VALSAMIS, MP
    [J]. ARCHIVES OF NEUROLOGY, 1976, 33 (02) : 120 - 130
  • [9] CHRONIC GM2 GANGLIOSIDOSIS MASQUERADING AS ATYPICAL FRIEDREICH ATAXIA - CLINICAL, MORPHOLOGIC, AND BIOCHEMICAL-STUDIES OF 9 CASES
    WILLNER, JP
    GRABOWSKI, GA
    GORDON, RE
    BENDER, AN
    DESNICK, RJ
    [J]. NEUROLOGY, 1981, 31 (07) : 787 - 798