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Autor:
Daly M, Dj, Perry, Db, Bruce, Pl, Harper, Robert Tait, Id, Walker, Ee, Mayne, Hm, Daly, Brown K, Rw, Carrell
Publikováno v:
Europe PubMed Central
The genetic basis of Type I antithrombin deficiency has been investigated in six unrelated kindred with positive histories of thrombosis using a PCR amplification/direct sequencing approach. Four frameshift mutations, all introducing premature transl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::884ddf4d2bacb9f007d51623569e3607
https://pubmed.ncbi.nlm.nih.gov/8735803
https://pubmed.ncbi.nlm.nih.gov/8735803
