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A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndrome
Author(s) -
Steindl K,
Alazami AM,
Bhatia KP,
Wuerfel JT,
Petersen D,
Cartolari R,
Neri G,
Klein C,
Mongiardo B,
Alkuraya FS,
Schneider SA
Publication year - 2010
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.2010.01447.x
Subject(s) - clonus , physical medicine and rehabilitation , gait , psychology , medicine , neuroscience , epilepsy