A New Locus-Specific Database (LSDB) for Mutations in the Folliculin (FLCN) Gene

D.H.K. Lim; P.K. Rehal; M.S. Nahorski; F. Macdonald; T. Claessens; M. Van Geel; L. Gijezen; J.J.P. Gille; S. Giraud; S. Richard; M. van Steensel; F.H. Menko; E.R. Maher

doi:10.1002/humu.21130

A New Locus-Specific Database (LSDB) for Mutations in the Folliculin (FLCN) Gene

D.H.K. Lim, P.K. Rehal, M.S. Nahorski, F. Macdonald, T. Claessens, M. Van Geel, L. Gijezen, J.J.P. Gille, S. Giraud, S. Richard, M. van Steensel, F.H. Menko, E.R. Maher

Clinical genetics

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

Original language	Undefined/Unknown
Pages (from-to)	E1043-E1051
Journal	Human Mutation
Volume	31
Issue number	1
DOIs	https://doi.org/10.1002/humu.21130
Publication status	Published - 2010

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10.1002/humu.21130

Cite this

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title = "A New Locus-Specific Database (LSDB) for Mutations in the Folliculin (FLCN) Gene",

author = "D.H.K. Lim and P.K. Rehal and M.S. Nahorski and F. Macdonald and T. Claessens and {Van Geel}, M. and L. Gijezen and J.J.P. Gille and S. Giraud and S. Richard and {van Steensel}, M. and F.H. Menko and E.R. Maher",

year = "2010",

doi = "10.1002/humu.21130",

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journal = "Human Mutation",

issn = "1059-7794",

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A New Locus-Specific Database (LSDB) for Mutations in the Folliculin (FLCN) Gene. / Lim, D.H.K.; Rehal, P.K.; Nahorski, M.S.; Macdonald, F.; Claessens, T.; Van Geel, M.; Gijezen, L.; Gille, J.J.P.; Giraud, S.; Richard, S.; van Steensel, M.; Menko, F.H.; Maher, E.R.

In: Human Mutation, Vol. 31, No. 1, 2010, p. E1043-E1051.

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

TY - JOUR

T1 - A New Locus-Specific Database (LSDB) for Mutations in the Folliculin (FLCN) Gene

AU - Lim, D.H.K.

AU - Rehal, P.K.

AU - Nahorski, M.S.

AU - Macdonald, F.

AU - Claessens, T.

AU - Van Geel, M.

AU - Gijezen, L.

AU - Gille, J.J.P.

AU - Giraud, S.

AU - Richard, S.

AU - van Steensel, M.

AU - Menko, F.H.

AU - Maher, E.R.

PY - 2010

Y1 - 2010

U2 - 10.1002/humu.21130

DO - 10.1002/humu.21130

M3 - Article

C2 - 19802896

VL - 31

SP - E1043-E1051

JO - Human Mutation

JF - Human Mutation

SN - 1059-7794

IS - 1

ER -