Rare double sex and mab-3-related transcription factor 1 regulatory variants in severe spermatogenic failure
A. C. Lima, F. Carvalho, J. Gonçalves, S. Fernandes, P. I. Marques, M. Sousa, A. Barros, S. Seixas, A. Amorim, D. F. Conrad, A. M. Lopes, 02.07.2015
LIMA, Ana Cristina, et al. Rare double sex and mab‐3‐related transcription factor 1 regulatory variants in severe spermatogenic failure. Andrology, 2015, 3. Jg., Nr. 5, S. 825-833.
Publication: https://doi.org/10.1111/andr.12063
Disclaimer
The publication Rare double sex and mab-3-related transcription factor 1 regulatory variants in severe spermatogenic failure by A. C. Lima, F. Carvalho, J. Gonçalves, S. Fernandes, P. I. Marques, M. Sousa, A. Barros, S. Seixas, A. Amorim, D. F. Conrad, A. M. Lopes is not published under an open access license. Therefore, only content curated by the MFGA team can be shown. For abstract, images and tables please follow the link to the original publication.
Curation by the MFGA team Relevant data sets presented in the publication have been identified. If possible, annotations (title, general information, conditions, processed tissue types and processed cell types) have been added based on information from the publication.
Data set 1: Screening of the DMRT1 sequence of 155 NOA patients by Sanger sequencing
Genome: Sanger Sequencing
Conditions
Human phenotype ontology | Participants | Comment |
---|---|---|
HP:0011961: Non-obstructive azoospermia | 155 | Portuguese men |
HP:control | 376 | 75 normozoospermic and 301 fertile Portuguese men |