Individual families And NotJan G. M. Klijn

List of bibliographic references

Number of relevant bibliographic references: 2.

Ident.	Authors (with country if any)	Title
001726	Nigel F. Clarke [Australie] ; Hanna Kolski [Canada] ; Danielle E. Dye ; Esther Lim ; Robert L. L. Smith [Australie] ; Rakesh Patel [Nouvelle-Zélande] ; Michael C. Fahey [Australie] ; Rémi Bellance ; Norma B. Romero [France] ; Edward S. Johnson [Canada] ; Annick Labarre-Vila [France] ; Nicole Monnier [France] ; Nigel G. Laing ; Kathryn N. North [Australie]	Mutations in TPM3 are a common cause of congenital fiber type disproportion
001C81	Carina Wallgren-Pettersson [Finlande] ; Katarina Pelin [Finlande] ; Pirta Hilpel [Finlande] ; Kati Donner [Finlande] ; Berardino Porfirio [Italie] ; Claudio Graziano [Italie] ; Kathryn J. Swoboda [États-Unis] ; Michel Fardeau [France] ; J. Andoni Urtizberea [France] ; Francesco Muntoni [Royaume-Uni] ; Caroline Sewry [Royaume-Uni] ; Victor Dubowitz [Royaume-Uni] ; Susan Iannaccone [États-Unis] ; Carlo Minetti [Italie] ; Marina Pedemonte [Italie] ; Marco Seri [Italie] ; Roberto Cusano [Italie] ; Martin Lammens [Belgique] ; Avril Castagna-Sloane [Canada] ; Alan H. Beggs [États-Unis] ; Nigel G. Laing [Australie] ; Albert De La Chapelle [Finlande]	Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy

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