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Delineation of clinical features in Wiedemann-Steiner syndrome caused by KMT2A mutations.

Pubmed ID: 
25810209
Year: 
2015
Month: 
MAR
Citation: 
Miyake N, Tsurusaki Y, Koshimizu E, Okamoto N, Kosho T, Brown NJ, Tan TY, Yap PJ, Suzumura H, Tanaka T, Nagai T, Nakashima M, Saitsu H, Niikawa N, Matsumoto N. Delineation of clinical features in Wiedemann-Steiner syndrome caused by KMT2A mutations. Clinical genetics (2015) PubMed