Journal Article

Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family

Asif Mir; Kumudesh Sritharan; Kirti Mittal; Nasim Vasli; Carolina Araujo; Talal Jamil; Muhammad Arshad Rafiq; Zubair Anwar; Anna Mikhailov; Sobiah Rauf; Huda Mahmood; Abdul Shakoor; Sabir Ali; Joyce So; Farooq Naeem; Muhammad Ayub; John B. Vincent

Human Genetics · Vol. 133, Issue 8 · pp. 975-984 · 2014

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Abstract

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Bibliographic Information

Journal	Human Genetics
Publisher	Springer
Publication Date	2014-08-01
Publication Year	2014
Volume	133
Issue	8
Pages	975-984
Document Type	Journal Article
Print ISSN	0340-6717
eISSN	1432-1203
DOI	10.1007/s00439-014-1438-0

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NARA Access Coverage	1964-01-01~Current
Journal Homepage	https://www.springer.com/journal/439
Publisher Page	Open Publisher Page

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