Deficiency in the endocytic adaptor proteins PHETA1/2 impairs renal and craniofacial development
A critical barrier in the treatment of endosomal and lysosomal diseases is the lack of understanding of the in vivo functions of the putative causative genes. We addressed this by investigating a key pair of endocytic adaptor proteins, PH domain-containing endocytic trafficking adaptor 1 and 2 (PHET...
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Main Authors: | , , , , , , , , , , , , , , , , , , , |
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Format: | Bog |
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The Company of Biologists,
2020-05-01T00:00:00Z.
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A1234.567 |
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