Autor: |
Hannah L. Marko, Nadine C. Hornig, Regina C. Betz, Paul‐Martin Holterhus, Janine Altmüller, Holger Thiele, Marietta Fabiano, Hans‐Udo Schweikert, Doreen Braun, Ulrich Schweizer |
Rok vydání: |
2021 |
Předmět: |
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Zdroj: |
Human mutationREFERENCES. 43(3) |
ISSN: |
1098-1004 |
Popis: |
Transporter-dependent steroid hormone uptake into target cells was demonstrated in genetically engineered mice and fruit flies. We hypothesized that mutations in such transporters may cause differences in sex development (DSD) in humans. Exome sequencing was performed in 16 genetically unsolved cases of 46,XY DSD selected from an anonymized collection of 708 lines of genital fibroblasts (GF) that were taken from individuals with incomplete virilization. Selection criteria were based on available biochemical characterization of GF compatible with reduced androgen uptake. Two unrelated individuals were identified with mutations in LDL receptor-related protein 2 (LRP2), a gene previously associated with partial sex steroid insensitivity in mice. Like Lrp2 |
Databáze: |
OpenAIRE |
Externí odkaz: |
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