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Q34339671-D96B3F14-8905-48DF-BE14-20E578196BE0
Q34339671-D96B3F14-8905-48DF-BE14-20E578196BE0
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http://www.wikidata.org/entity/statement/Q34339671-D96B3F14-8905-48DF-BE14-20E578196BE0
Human RTEL1 deficiency causes Hoyeraal-Hreidarsson syndrome with short telomeres and genome instability.
P2860
Q34339671-D96B3F14-8905-48DF-BE14-20E578196BE0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34339671-D96B3F14-8905-48DF-BE14-20E578196BE0
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wasDerivedFrom
be51bee7a9ce449e521d3d4b36e6a45eb0d94932
P2860
XPD helicase structures and activities: insights into the cancer and aging phenotypes from XPD mutations