Recurrent mutation 4882delTT in the GAP-related domain of the tuberous sclerosis TSC2 gene

S Verhoef; R Vrtel; CE Bakker; I Stolte-Dijkstra; Mark Nellist; JH Begeer; J Zaremba; S Jozwiak; AMP (Anita) Tempelaars; D (Dick) Lindhout; Dicky Halley; Ans van den Ouweland

Recurrent mutation 4882delTT in the GAP-related domain of the tuberous sclerosis TSC2 gene

S Verhoef
, R Vrtel
, CE Bakker
, I Stolte-Dijkstra
, Mark Nellist
, JH Begeer
, J Zaremba
, S Jozwiak
, AMP (Anita) Tempelaars
, D (Dick) Lindhout
, Dicky Halley
, Ans van den Ouweland

Clinical Genetics

External organisation

Research output: Contribution to journal › Article › Academic › peer-review

10 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	85-87
Number of pages	3
Journal	Human Mutation
Volume	suppl. 1
Publication status	Published - 1998

Research programs

EMC MGC-02-96-01

Cite this

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title = "Recurrent mutation 4882delTT in the GAP-related domain of the tuberous sclerosis TSC2 gene",

author = "S Verhoef and R Vrtel and CE Bakker and I Stolte-Dijkstra and Mark Nellist and JH Begeer and J Zaremba and S Jozwiak and Tempelaars, \{AMP (Anita)\} and Lindhout, \{D (Dick)\} and Dicky Halley and \{van den Ouweland\}, Ans",

year = "1998",

language = "Undefined/Unknown",

volume = "suppl. 1",

pages = "85--87",

journal = "Human Mutation",

issn = "1059-7794",

publisher = "John Wiley \& Sons Inc.",

}

TY - JOUR

T1 - Recurrent mutation 4882delTT in the GAP-related domain of the tuberous sclerosis TSC2 gene

AU - Verhoef, S

AU - Vrtel, R

AU - Bakker, CE

AU - Stolte-Dijkstra, I

AU - Nellist, Mark

AU - Begeer, JH

AU - Zaremba, J

AU - Jozwiak, S

AU - Tempelaars, AMP (Anita)

AU - Lindhout, D (Dick)

AU - Halley, Dicky

AU - van den Ouweland, Ans

PY - 1998

Y1 - 1998

M3 - Article

SN - 1059-7794

VL - suppl. 1

SP - 85

EP - 87

JO - Human Mutation

JF - Human Mutation

ER -