SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype

G Spurlock; E Bennett; N Chuzhanova; N Thomas; Jim H-Ping; L Side; S Davies; Eric Haan; B Kerr; S Huson; M Upadhyaya

SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype

G Spurlock, E Bennett, N Chuzhanova, N Thomas, Jim H-Ping, L Side, S Davies, Eric Haan, B Kerr, S Huson, M Upadhyaya

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

70 Citations (Scopus)

Original language	English
Pages (from-to)	431-437
Number of pages	7
Journal	Journal of Medical Genetics
Volume	46
Publication status	Published - 2009

Cite this

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title = "SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype",

author = "G Spurlock and E Bennett and N Chuzhanova and N Thomas and Jim H-Ping and L Side and S Davies and Eric Haan and B Kerr and S Huson and M Upadhyaya",

year = "2009",

language = "English",

volume = "46",

pages = "431--437",

journal = "Journal of Medical Genetics",

issn = "0022-2593",

publisher = "BMJ PUBLISHING",

}

TY - JOUR

T1 - SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype

AU - Spurlock, G

AU - Bennett, E

AU - Chuzhanova, N

AU - Thomas, N

AU - H-Ping, Jim

AU - Side, L

AU - Davies, S

AU - Haan, Eric

AU - Kerr, B

AU - Huson, S

AU - Upadhyaya, M

PY - 2009

Y1 - 2009

M3 - Article

SN - 0022-2593

VL - 46

SP - 431

EP - 437

JO - Journal of Medical Genetics

JF - Journal of Medical Genetics

ER -