Extensive Variation in the Mutation Rate Between and Within Human Genes Associated with Mendelian Disease

T Smith; G Ho; J Christodoulou; E A Price; Z Onadim; M Gauthier-Villars; C Dehainault; C Houdayer; B Parfait; Rick van Minkelen; D Lohman; A Eyre-Walker

doi:10.1002/humu.22967

Extensive Variation in the Mutation Rate Between and Within Human Genes Associated with Mendelian Disease

T Smith
, G Ho
, J Christodoulou
, E A Price
, Z Onadim
, M Gauthier-Villars
, C Dehainault
, C Houdayer
, B Parfait
, Rick van Minkelen
, D Lohman
, A Eyre-Walker

Clinical Genetics

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

11 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	488-494
Number of pages	7
Journal	Human Mutation
Volume	37
Issue number	5
DOIs	https://doi.org/10.1002/humu.22967
Publication status	Published - 2016

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being

Research programs

EMC MGC-02-96-01

Access to Document

10.1002/humu.22967

Cite this

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title = "Extensive Variation in the Mutation Rate Between and Within Human Genes Associated with Mendelian Disease",

author = "T Smith and G Ho and J Christodoulou and Price, \{E A\} and Z Onadim and M Gauthier-Villars and C Dehainault and C Houdayer and B Parfait and \{van Minkelen\}, Rick and D Lohman and A Eyre-Walker",

year = "2016",

doi = "10.1002/humu.22967",

language = "Undefined/Unknown",

volume = "37",

pages = "488--494",

journal = "Human Mutation",

issn = "1059-7794",

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

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}

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T1 - Extensive Variation in the Mutation Rate Between and Within Human Genes Associated with Mendelian Disease

AU - Smith, T

AU - Ho, G

AU - Christodoulou, J

AU - Price, E A

AU - Onadim, Z

AU - Gauthier-Villars, M

AU - Dehainault, C

AU - Houdayer, C

AU - Parfait, B

AU - van Minkelen, Rick

AU - Lohman, D

AU - Eyre-Walker, A

PY - 2016

Y1 - 2016

U2 - 10.1002/humu.22967

DO - 10.1002/humu.22967

M3 - Article

C2 - 26857394

SN - 1059-7794

VL - 37

SP - 488

EP - 494

JO - Human Mutation

JF - Human Mutation

IS - 5

ER -