HIGHLIGHTS
- who: McLeod syndrome et al. from the SRK, Switzerland Istanbul University, Tu00fcrkiye have published the article: A case of McLeod syndrome caused by a nonsense variation c.942G A in the gene: A case report, in the Journal: (JOURNAL) of 26/06/2020
- how: The sequencing results showed that the patient carried a hemizygous c.942G>A variation in the XK gene corresponding to the XK*N.47 allele in the International Society of Subsequently the coding region sequence of exons 1-3 in the XK gene was amplified by a polymerase_chain_reaction in the laboratory . . .
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