ONSET IN THE 7TH DECADE AND LACK OF SYMPTOMS IN HETEROZYGOTES FOR THE TTRMET30 MUTATION IN HEREDITARY AMYLOID NEUROPATHY - TYPE-I (PORTUGUESE, ANDRADE)

被引:38
作者
SEQUEIROS, J
SARAIVA, MJM
机构
[1] UNIV PORTO,INST CIENCIAS BIOMED ABEL SALAZAR,BIOQUIM LAB,P-4000 PORTO,PORTUGAL
[2] JOHNS HOPKINS UNIV,SCH MED,DEPT MED,DIV MED GENET,BALTIMORE,MD 21205
[3] COLUMBIA UNIV COLL PHYS & SURG,DEPT MED,DIV METAB,NEW YORK,NY 10032
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1987年 / 27卷 / 02期
关键词
D O I
10.1002/ajmg.1320270213
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:345 / 357
页数:13
相关论文
共 48 条
[1]  
Andersson R, 1976, Acta Med Scand Suppl, V590, P1
[3]   GENETIC ASPECT FO FAMILIAN AMYLOIDOTIC POLYNEUROPATHY - PORTUGUESE TYPE OF PARAMYLOIDOSIS [J].
ANDRADE, C ;
CANIJO, M ;
KLEIN, D ;
KAELIN, A .
HUMANGENETIK, 1969, 7 (02) :163-&
[4]   HEREDITARY AMYLOIDOSIS [J].
ANDRADE, C ;
ARAKI, S ;
BLOCK, WD ;
COHEN, AS ;
JACKSON, CE ;
KUROIWA, Y ;
MCKUSICK, VA ;
NISSIM, J ;
SOHAR, E ;
VANALLEN, MW .
ARTHRITIS AND RHEUMATISM, 1970, 13 (06) :902-&
[5]  
ANDRADE C, 1975, HDB CLIN NEUROLOGY, V21, P119
[6]  
BECKER PE, 1964, Z MENSCH VERERB KONS, V37, P329
[7]  
BENSON MD, 1985, CLIN RES, V33, pA590
[8]   PARTIAL AMINO-ACID-SEQUENCE HOMOLOGY BETWEEN AN HEREDOFAMILIAL AMYLOID PROTEIN AND HUMAN-PLASMA PRE-ALBUMIN [J].
BENSON, MD .
JOURNAL OF CLINICAL INVESTIGATION, 1981, 67 (04) :1035-1041
[9]  
BERGAMINI L, 1978, PERIPHERAL NEUROPATH, P413
[10]   PERIPHERAL-NERVE FIBER CHANGES IN ASYMPTOMATIC CHILDREN OF PATIENTS WITH FAMILIAL AMYLOID POLYNEUROPATHY [J].
CARVALHO, J ;
COIMBRA, A ;
ANDRADE, C .
BRAIN, 1976, 99 (MAR) :1-10