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Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2

✍ Scribed by Jaume Colomer; Rebecca Gooding; Dora Angelicheva; Rosalind H.M. King; Encarna Guillén-Navarro; Yesim Parman; Andres Nascimento; Joan Conill; Luba Kalaydjieva


Book ID
116792463
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
77 KB
Volume
16
Category
Article
ISSN
0960-8966

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