Novel truncating and missense mutations of the KCC3 gene associated with Andermann syndrome.

scientific article

Novel truncating and missense mutations of the KCC3 gene associated with Andermann syndrome. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1212/01.WNL.0000204181.31175.8B
P698PubMed publication ID16606917

P50authorBeate WinnerQ56441815
P2093author name stringWinkler J
Gross C
Bogdahn U
Demir E
Hehr U
Uyanik G
Olmez A
Wahl D
Yilmaz Y
Topaloglu H
Elcioglu N
Penzien J
Scheglmann K
P433issue7
P407language of work or nameEnglishQ1860
P304page(s)1044-1048
P577publication date2006-04-01
P1433published inNeurologyQ1161692
P1476titleNovel truncating and missense mutations of the KCC3 gene associated with Andermann syndrome
P478volume66

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cites work (P2860)
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