New SMS mutation leads to a striking reduction in spermine synthase protein function and a severe form of Snyder-Robinson X-linked recessive mental retardation syndrome.

scientific article published on 11 June 2008

New SMS mutation leads to a striking reduction in spermine synthase protein function and a severe form of Snyder-Robinson X-linked recessive mental retardation syndrome. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1136/JMG.2007.056713
P698PubMed publication ID18550699

P50authorDébora R BertolaQ51915156
Maria Rita Passos-BuenoQ78114430
P2093author name stringX Wang
C E Schwartz
A E Pegg
D E McCloskey
A L Sertié
C M C Maranduba
G de Alencastro
S E Kliemann
P433issue8
P407language of work or nameEnglishQ1860
P304page(s)539-543
P577publication date2008-06-11
P1433published inJournal of Medical GeneticsQ14640281
P1476titleNew SMS mutation leads to a striking reduction in spermine synthase protein function and a severe form of Snyder-Robinson X-linked recessive mental retardation syndrome
P478volume45