GENETIC DISEASES OF METABOLISM

被引：33

作者：

RAIVIO, KO

SEEGMILLER, JE

机构：

来源：

ANNUAL REVIEW OF BIOCHEMISTRY | 1972年 / 41卷

关键词：

D O I：

10.1146/annurev.bi.41.070172.002551

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：543 / +

页数：1

共 288 条

[1] OBSERVATIONS IN 2 SWISS FAMILIES WITH ACATALASIA .2. [J].

AEBI, H ;

BAGGIOLINI, M ;

DEWALD, B ;

LAUBER, E ;

SUTER, H ;

MICHELI, A ;

FREI, J .

ENZYMOLOGIA BIOLOGICA ET CLINICA, 1964, 4 (03) :121-151

[2] INBORN ERRORS OF METABOLISM [J].

AEBI, HE .

ANNUAL REVIEW OF BIOCHEMISTRY, 1967, 36 :271-+

[3] EFFECT OF PHENYLALANINE ON PROTEIN SYNTHESIS IN DEVELOPING RAT BRAIN [J].

AGRAWAL, HC ;

BONE, AH ;

DAVISON, AN .

BIOCHEMICAL JOURNAL, 1970, 117 (02) :325-&

[4] METABOLISM OF GLYCINE IN NONKETOTIC FORM OF HYPERGLYCINEMIA [J].

ANDO, T ;

NYHAN, WL ;

GERRITSEN, T ;

GONG, L ;

HEINER, DC ;

BRAY, PF .

PEDIATRIC RESEARCH, 1968, 2 (04) :254-+

[5]

APPEL SH, 1965, J CLIN INVEST, V44, P1026

[6]

APPEL SH, 1968, J BIOL CHEM, V243, P3924

[7] CONGENITAL DEFECT IN FOLATE UTILIZATION [J].

ARAKAWA, T .

AMERICAN JOURNAL OF MEDICINE, 1970, 48 (05) :594-&

[8] CHRONIC NONHEMOLYTIC UNCONJUGATED HYPERBILIRUBINEMIA WITH GLUCURONYL TRANSFERASE DEFICIENCY - CLINICAL, BIOCHEMICAL, PHARMACOLOGIC AND GENETIC EVIDENCE FOR HETEROGENEITY [J].

ARIAS, IM ;

GARTNER, LM ;

COHEN, M ;

EZZER, JB ;

LEVI, AJ .

AMERICAN JOURNAL OF MEDICINE, 1969, 47 (03) :395-&

[9]

ARONSON NN, 1968, J BIOL CHEM, V243, P4494

[10]

ARONSON SM, 1964, TAYSACHS DISEASE, P118

← 1 2 3 4 5 6 7 8 9 10 →