PHENYLKETONURIA AND OTHER PHENYLALANINE HYDROXYLATION MUTANTS IN MAN

被引：63

作者：

SCRIVER, CR

CLOW, CL

机构：

[1] MCGILL UNIV, DEPT PEDIAT, MONTREAL H3C 3G1, QUEBEC, CANADA

[2] MCGILL UNIV, CTR HUMAN GENET, MONTREAL H3C 3G1, QUEBEC, CANADA

[3] MCGILL UNIV, MONTREAL CHILDRENS HOSP, RES INST, DE BELLE LAB BIOCHEM GENET, MONTREAL H3H 1P3, QUEBEC, CANADA

来源：

关键词：

D O I：

10.1146/annurev.ge.14.120180.001143

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：179 / 202

页数：24

共 120 条

[81]

NIEDERWIESER A, 1979, FOLIC ACID NEUROLOGY, P349

[82]

NIELSEN KB, 1979, LANCET, V1, P1245

[83]

PAUL TD, 1979, AM J HUM GENET, V31, pA140

[84]

PAUL TD, 1978, AM J HUM GENET, V30, P293

[85]

PAUL TD, 1979, CLIN GENET, V16, P217

[86]

Pfleiderer W, 1978, J Inherit Metab Dis, V1, P54, DOI 10.1007/BF01801844

PUESCHEL, SM ;

HUM, C ;

ANDREWS, M .

[88]

RAO DC, 1979, AM J HUM GENET, V31, P680

[89]

Rembold H, 1978, J Inherit Metab Dis, V1, P61, DOI 10.1007/BF01801845

[90]

REY F, 1977, ARCH FR PEDIATR, V34, P109