Premium
High frequency of p.Thr93Met in Smith‐Lemli‐Opitz syndrome patients in Turkey
Author(s) -
Kalb S,
Caglayan AO,
Degerliyurt A,
Schmid S,
Ceylaner S,
Hatipoglu N,
Hinderhofer K,
Rehder H,
Kurtoglu S,
Ceylaner G,
Zschocke J,
WitschBaumgartner M
Publication year - 2012
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.1399-0004.2011.01750.x
Subject(s) - medical genetics , medicine , human genetics , pediatric neurology , pediatrics , genetics , biology , gene