Gonadotropin-releasing hormone receptor gene mutation: A new cause of hereditary hypogonadism and another mutated G-protein-coupled receptor

被引：5

作者：

Bertherat, J ^{[1
]}

机构：

[1] Hop Cochin, Malad Endocriniennes & Metab Clin, F-75014 Paris, France

来源：

EUROPEAN JOURNAL OF ENDOCRINOLOGY | 1998年 / 138卷 / 06期

关键词：

D O I：

10.1530/eje.0.1380621

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：621 / 622

页数：2

共 7 条

[1] INTRAGENIC DELETION OF THE KALIG-1 GENE IN KALLMANNS SYNDROME [J].

BICK, D ;

FRANCO, B ;

SHERINS, RJ ;

HEYE, B ;

PIKE, L ;

CRAWFORD, J ;

MADDALENA, A ;

INCERTI, B ;

PRAGLIOLA, A ;

MEITINGER, T ;

BALLABIO, A .

NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (26) :1752-1755

[2] A family with hypogonadotropic hypogonadism and mutations in the gonadotropin-releasing hormone receptor [J].

deRoux, N ;

Young, J ;

Misrahi, M ;

Genet, R ;

Chanson, P ;

Schaison, G ;

Milgrom, E .

NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (22) :1597-1602

[3] Mutations in gonadotropin-releasing hormone receptor gene cause hypogonadotropic hypogonadism [J].

Layman, LC ;

Cohen, DP ;

Jin, M ;

Xie, J ;

Li, Z ;

Reindollar, RH ;

Bolbolan, S ;

Bick, DP ;

Sherins, RR ;

Duck, LW ;

Musgrove, LC ;

Sellers, JC ;

Neill, JD .

NATURE GENETICS, 1998, 18 (01) :14-15

[4]

MASSON AJ, 1986, SCIENCE, V234, P1366

[5]

MEITINGER T, 1990, AM J HUM GENET, V47, P664

[6] NORMAL STRUCTURE OF THE GONADOTROPIN-RELEASING HORMONE (GNRH) GENE IN PATIENTS WITH GNRH DEFICIENCY AND IDIOPATHIC HYPOGONADOTROPIC HYPOGONADISM [J].

WEISS, J ;

CROWLEY, WF ;

JAMESON, JL .

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1989, 69 (02) :299-303

[7] AN UNUSUAL MEMBER OF THE NUCLEAR HORMONE-RECEPTOR SUPERFAMILY RESPONSIBLE FOR X-LINKED ADRENAL HYPOPLASIA CONGENITA [J].

ZANARIA, E ;

MUSCATELLI, F ;

BARDONI, B ;

STROM, TM ;

GUIOLI, S ;

GUO, WW ;

LALLI, E ;

MOSER, C ;

WALKER, AP ;

MCCABE, ERB ;

MEITINGER, T ;

MONACO, AP ;

SASSONECORSI, P ;

CAMERINO, G .

NATURE, 1994, 372 (6507) :635-641

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