Novel truncating mutation in TENM3 in siblings with motor developmental delay, ocular coloboma, oval cornea, without microphthalmia. [electronic resource]

By: Contributor(s): Producer: 20191029Description: 2930-2933 p. digitalISSN:
  • 1552-4833
Subject(s): Online resources: In: American journal of medical genetics. Part A vol. 176
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Publication Type: Case Reports; Letter; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't; Review

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