Mutations in a novel primate-specific cryptic exon of the LHCGR gene cause Leydig cell hypoplasia

被引：0

|

作者：

Kossack, N.

Simoni, M.

Richter-Unruh, A.

机构：

[1] Inst Reprod Med, Munster, Germany

[2] Endokrinol Ruhr, Bochum, Germany

来源：

EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES | 2007年 / 115卷

关键词：

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

收藏

页码：S12 / S12

页数：1

相关论文

共 44 条

[41] NOVEL TESTIS GERM CELL-SPECIFIC TRANSCRIPT OF THE CREB GENE CONTAINS AN ALTERNATIVELY SPLICED EXON WITH MULTIPLE IN-FRAME STOP CODONS
WAEBER, G
HABENER, JF
ENDOCRINOLOGY, 1992, 131 (04) : 2010 - 2015
[42] Multiple exon screening using restriction endonuclease fingerprinting (REF): Detection of six novel mutations in the L1 cell adhesion molecule (L1CAM) gene
Du, YZ
Srivastava, AK
Schwartz, CE
HUMAN MUTATION, 1998, 11 (03) : 222 - 230
[43] Mutations in the rod photoreceptor cell-specific ATP-binding cassette transporter (ABCR) gene are a major cause of autosomal recessive cone-rod dystrophy.
Maugeri, A
Klevering, BJ
Rohrschneider, K
Blankenagel, A
Deutman, AF
Hoyng, CB
Cremers, FPM
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2000, 41 (04) : S95 - S95
[44] Novel PAMs from somatic mutations produce numerous pancreatic cancer-specific CRISPR-Cas9 targets for selective cell elimination: A novel gene therapy approach for cancer
Teh, Selina Shiqing K.
Bowland, Kirsten
Bennett, Alexis
Halper-Stromberg, Eitan
Skaist, Alyza
Pallavajjala, Aparna
Tang, Jacqueline
Cai, Fidel
Liang, Hong
Wheelan, Sarah
Scharpf, Robert B.
Roberts, Nicholas J.
Eshleman, James R.
MOLECULAR CANCER THERAPEUTICS, 2023, 22 (12)

← 1 2 3 4 5 →