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2023 | 1 |
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Deficiency of the mitochondrial ribosomal subunit, MRPL50, causes autosomal recessive syndromic premature ovarian insufficiency.
Hum Genet. 2023 Jul;142(7):879-907. doi: 10.1007/s00439-023-02563-z. Epub 2023 May 6.
Hum Genet. 2023.
PMID: 37148394
Free PMC article.
A Human Homozygous HELQ Missense Variant Does Not Cause Premature Ovarian Insufficiency in a Mouse Model.
Bakhshalizadeh S, Bird AD, Sreenivasan R, Bell KM, Robevska G, van den Bergen J, Asghari-Jafarabadi M, Kueh AJ, Touraine P, Lokchine A, Jaillard S, Ayers KL, Wilhelm D, Sinclair AH, Tucker EJ.
Bakhshalizadeh S, et al.
Genes (Basel). 2024 Mar 4;15(3):333. doi: 10.3390/genes15030333.
Genes (Basel). 2024.
PMID: 38540391
Free PMC article.
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Functional characterization of human recessive DIS3 variants in premature ovarian insufficiency†.
Kline BL, Siddall NA, Wijaya F, Stuart CJ, Orlando L, Bakhshalizadeh S, Afkhami F, Bell KM, Jaillard S, Robevska G, van den Bergen JA, Shahbazi S, van Hoof A, Ayers KL, Hime GR, Sinclair AH, Tucker EJ.
Kline BL, et al.
Biol Reprod. 2025 Jan 14;112(1):102-118. doi: 10.1093/biolre/ioae148.
Biol Reprod. 2025.
PMID: 39400047
Free PMC article.
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