Wikidata

(Q80604139)

English

Familial haemophagocytic lymphohistiocytosis in patients who are heterozygous for the A91V perforin variation is often associated with other genetic defects

scientific article published on 01 August 2007

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title
Familial haemophagocytic lymphohistiocytosis in patients who are heterozygous for the A91V perforin variation is often associated with other genetic defects (English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
17627755
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17627755%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 January 2020
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