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Functional characterization of the TSC2 c.3598C>T (p.R1200W) missense mutation that co-segregates with tuberous sclerosis complex in mildly affected kindreds

✍ Scribed by M Wentink; M Nellist; M Hoogeveen-Westerveld; B Zonnenberg; D van der Kolk; T van Essen; S-M Park; G Woods; P Cohn-Hokke; W Brussel; E Smeets; A Brooks; D Halley; A van den Ouweland; A Maat-Kievit


Book ID
115091941
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
774 KB
Volume
81
Category
Article
ISSN
0009-9163

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