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Recurrent mutation 4882delTT in the GAP‐related domain of the tuberous sclerosis TSC2 gene
Author(s) -
Verhoef S.,
Vrtel R.,
Bakker L.,
StolteDijkstra I.,
Nellist M.,
Begeer J.H.,
Zaremba J.,
Jozwiak S.,
Tempelaars A.M.P.,
Lindhout D.,
Halley D.J.J.,
van den Ouweland A.M.W.
Publication year - 1998
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/humu.1380110129
Subject(s) - erasmus+ , rotterdam study , medicine , art history , history , disease , the renaissance