Biallelic loss of function variants in PPP1R21 cause a neurodevelopmental syndrome with impaired endocytic function

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Publication year
2019
Author(s)
Rehman, Atteeq U.
Najafi, Maryam
Kambouris, Marios
Al-Gazali, Lihadh
Makrythanasis, Periklis
Rad, Abolfazl
Bakey, Z.
Wu, K.M.
Yang, Yaping
Schmidts, M.
Source
Human Mutation, 40, 3, (2019), pp. 267-280
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Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/201369   https://hdl.handle.net/2066/201369
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