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Year | Number of Results |
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1996 | 1 |
2000 | 1 |
2001 | 2 |
2019 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 28957
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Mutations in the MRPS28 gene encoding the small mitoribosomal subunit protein bS1m in a patient with intrauterine growth retardation, craniofacial dysmorphism and multisystemic involvement.
Hum Mol Genet. 2019 May 1;28(9):1445-1462. doi: 10.1093/hmg/ddy441.
Hum Mol Genet. 2019.
PMID: 30566640
The human mitochondrial ribosomal protein genes: mapping of 54 genes to the chromosomes and implications for human disorders.
Kenmochi N, Suzuki T, Uechi T, Magoori M, Kuniba M, Higa S, Watanabe K, Tanaka T.
Kenmochi N, et al.
Genomics. 2001 Sep;77(1-2):65-70. doi: 10.1006/geno.2001.6622.
Genomics. 2001.
PMID: 11543634
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The small subunit of the mammalian mitochondrial ribosome. Identification of the full complement of ribosomal proteins present.
Cavdar Koc E, Burkhart W, Blackburn K, Moseley A, Spremulli LL.
Cavdar Koc E, et al.
J Biol Chem. 2001 Jun 1;276(22):19363-74. doi: 10.1074/jbc.M100727200. Epub 2001 Mar 2.
J Biol Chem. 2001.
PMID: 11279123
Free article.
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Mammalian mitochondrial ribosomal proteins (4). Amino acid sequencing, characterization, and identification of corresponding gene sequences.
O'Brien TW, Liu J, Sylvester JE, Mougey EB, Fischel-Ghodsian N, Thiede B, Wittmann-Liebold B, Graack HR.
O'Brien TW, et al.
J Biol Chem. 2000 Jun 16;275(24):18153-9. doi: 10.1074/jbc.M909762199.
J Biol Chem. 2000.
PMID: 10751423
Free article.
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Craniofacial anomalies and malformations in respiratory chain deficiency.
Cormier-Daire V, Rustin P, Rötig A, Chrétien D, Le Merrer M, Belli D, Le Goff A, Hubert P, Ricour C, Munnich A.
Cormier-Daire V, et al.
Am J Med Genet. 1996 Dec 30;66(4):457-63. doi: 10.1002/(SICI)1096-8628(19961230)66:4<457::AID-AJMG15>3.0.CO;2-T.
Am J Med Genet. 1996.
PMID: 8989468
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