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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