Published in
Wiley, Human Mutation: Variation, Informatics and Disease, 2018
DOI: 10.1002/humu.23694
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Biallelic loss of function variants in PPP1R21 cause a neurodevelopmental syndrome with impaired endocytic function
Journal article published in 2018 by
Atteeq U. Rehman,
Maryam Najafi,
Marios Kambouris,
Lihadh Al Gazali 
,
Periklis Makrythanasis,
Abolfazl Rad,
Reza Maroofian,
Anna Rajab,
Zornitza Stark,
Jill V. Hunter,
Zeineb Bakey,
Mari J. Tokita,
Weimin He,
Francesco Vetrini,
Andrea Petersen
and other authors.
,
Periklis Makrythanasis,
Abolfazl Rad,
Reza Maroofian,
Anna Rajab,
Zornitza Stark,
Jill V. Hunter,
Zeineb Bakey,
Mari J. Tokita,
Weimin He,
Francesco Vetrini,
Andrea Petersen
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
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