Exome Sequencing Reveals Variants In Known And Novel Candidate Genes For Severe Sperm Motility Disorders

EUROPEAN JOURNAL OF HUMAN GENETICS(2020)

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摘要
This project was supported in part by funding from the Australian National Health and Medical Research Council (APP1120356) to M.K.O.B., J.A.V. and R.I.M.L., The Netherlands Organisation for Scientific Research (918-15-667) to J.A.V., the Royal Society and Wolfson Foundation (WM160091) to J.A.V., as well as an Investigator Award in Science from the Wellcome Trust (209451) to J.A.V. and Grants from the National Research Council of Argentina (PIP 0900 and 4584) and ANPCyT (PICT 9591) to H.E.C. and a UUKi Rutherford Fund Fellowship awarded to B.J.H.
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关键词
asthenozoospermia,candidate novel genes,dysplasia of the fibrous sheath,male infertility,multiple morphological abnormalities of the sperm flagella,sperm motility disorders,whole exome sequencing
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