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🚀🌠 Tremendous Traffic: 10M - 20M visitors per month


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Earning money isn't the goal of every website; some are designed to offer support or promote social causes. People have different reasons for creating websites. This might be one such reason. Ncbi.nlm.nih.gov might be plotting its profit, but the way they're doing it isn't detectable yet.

Keywords {🔍}

ftsj, exon, protein, family, patient, doi, affected, pubmed, google, scholar, brain, mutation, human, pmc, mutations, mental, retardation, rna, mrx, sequence, control, gene, families, iii, fig, nsxlmr, methyltransferase, nlm, xlinked, shown, genes, deletion, coli, ftsjrrmj, age, cell, yeast, pintard, function, accession, male, nucleotides, ncbi, search, genet, article, expression, transcripts, xlmr, mild,

Topics {✒️}

s-adenosyl-l-methionine–dependent methyltransferases bind s-adenosyl-l-methionine x-linked mental retardation s-adomet–binding domain heat-induced rrna methyltransferase cryptic splice-site activation s-adenosylmethionine–binding protein pmc copyright notice pmc beta search coli ftsj/rrmj protein mutant rt-pcr products license information pmcid regular primary school mental retardation highlights snr52-dependent mechanism heat shock control coli ftsj/rrmj moderate mental retardation β-actin served european mrx consortium ftsj/rrmj homologs ftsj/rrmj gene pcr-amplified ftsj1 transcripts 21s rrna methylation publisher site pdf hans van bokhoven 5 medical research council splice-site mutation ribose 2′-o-methyltransferases +-binding protein pab1p 744-bp cdna probe 25s rrna synthesis yeast nucleolar protein rrmj/fibrillarin superfamily work education program ribosomal rna methyltransferase rt-pcr products ftsj1-specific probe current studies aim conserved rrna position mutant ftsj1 transcripts performed northern blotting united states government vincent des portes 4 receiving informed consent obligate female carriers specific product revealed premature stop codon significantly reduced level c-terminal part

Questions {❓}

• Ropers HH, Hoeltzenbein M, Kalscheuer V, Yntema H, Hamel B, Fryns JP, Chelly J, Partington M, Gecz J, Moraine C (2003) Nonsyndromic X-linked mental retardation: where are the missing mutations?

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