Recurrent Mutation 4882delTT in the GAP-Related Domain of the Tuberous Sclerosis TSC2 Gene

S Verhoef; R Vrtel; L 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, L 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

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

Original language	Undefined/Unknown
Pages (from-to)	85-87
Number of pages	3
Journal	Human Mutation
Issue number	supplement
Publication status	Published - 1997

Research programs

EMC MGC-02-96-01

Cite this

@article{84fb1fc8abb84620807e12384dc9a3d6,

title = "Recurrent Mutation 4882delTT in the GAP-Related Domain of the Tuberous Sclerosis TSC2 Gene",

author = "S Verhoef and R Vrtel and L 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 = "1997",

language = "Undefined/Unknown",

pages = "85--87",

journal = "Human Mutation",

issn = "1059-7794",

publisher = "John Wiley & Sons Inc.",

number = "supplement",

}

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, L

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 - 1997

Y1 - 1997

M3 - Article

SN - 1059-7794

SP - 85

EP - 87

JO - Human Mutation

JF - Human Mutation

IS - supplement

ER -