Identification of a large insertion and two novel point mutations (3671del8 and S1221X) in tuberous sclerosis complex (TSC)

Q (Qing) Wang; S Verhoef; AMP (Anita) Tempelaars; PLG Bakker; R Vrtel; ALW Hesseling-Janssen; Mark Nellist; Arnold Oranje; H (Hans) Stroink; D (Dick) Lindhout; Dicky Halley; Ans van den Ouweland

Identification of a large insertion and two novel point mutations (3671del8 and S1221X) in tuberous sclerosis complex (TSC)

Q (Qing) Wang, S Verhoef, AMP (Anita) Tempelaars, PLG Bakker, R Vrtel, ALW Hesseling-Janssen, Mark Nellist, Arnold Oranje, H (Hans) Stroink, D (Dick) Lindhout, Dicky Halley, Ans van den Ouweland

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

Original language	Undefined/Unknown
Pages (from-to)	331-334
Number of pages	4
Journal	Human Mutation
Volume	11
Publication status	Published - 1997

Research programs

EMC MGC-02-96-01

Cite this

@article{c1e173be8bd645f291ea08e12ab21938,

title = "Identification of a large insertion and two novel point mutations (3671del8 and S1221X) in tuberous sclerosis complex (TSC)",

author = "Wang, {Q (Qing)} and S Verhoef and Tempelaars, {AMP (Anita)} and PLG Bakker and R Vrtel and ALW Hesseling-Janssen and Mark Nellist and Arnold Oranje and Stroink, {H (Hans)} and Lindhout, {D (Dick)} and Dicky Halley and {van den Ouweland}, Ans",

year = "1997",

language = "Undefined/Unknown",

volume = "11",

pages = "331--334",

journal = "Human Mutation",

issn = "1059-7794",

publisher = "John Wiley & Sons Inc.",

}

TY - JOUR

T1 - Identification of a large insertion and two novel point mutations (3671del8 and S1221X) in tuberous sclerosis complex (TSC)

AU - Wang, Q (Qing)

AU - Verhoef, S

AU - Tempelaars, AMP (Anita)

AU - Bakker, PLG

AU - Vrtel, R

AU - Hesseling-Janssen, ALW

AU - Nellist, Mark

AU - Oranje, Arnold

AU - Stroink, H (Hans)

AU - Lindhout, D (Dick)

AU - Halley, Dicky

AU - van den Ouweland, Ans

PY - 1997

Y1 - 1997

M3 - Article

SN - 1059-7794

VL - 11

SP - 331

EP - 334

JO - Human Mutation

JF - Human Mutation

ER -