De novo heterozygous missense and loss‐of‐function variants in CDC42BPB are associated with a neurodevelopmental phenotype
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W. Chung | E. Roeder | C. Saunders | I. Thiffault | D. Campion | C. Depienne | K. Gripp | M. Srour | K. Lichtenbelt | A. Selicorni | A. Larson | G. Hoganson | A. Accogli | D. Heron | A. Goldenberg | K. V. van Gassen | V. Okur | D. Niyazov | C. Nava | G. Sébire | Ilana Chilton | E. Rush | M. Mariani | J. Alaimo | S. Heide | G. Vitiello | M. Steinraths | Thomas Husson | J. Jenkins | R.O. Littlejohn | J. Fleischer | D. Groepper | J. Burton | Meron Azage | J. Rice | Jennifer Rice