Roos, A.; Senderek, J.; Cox, D.; Wiessner, M.; Zahedi, R.; Charlton, R.; Barresi, R.; Hathazi, D. and Lochmüller, H.
(2017):
Autosomal recessive myopathy associated with cataracts and learning difficulties caused by INPP5K mutations: a new syndromic gene linking four overlapping rare recessive neuromuscular disorders.
In: Neuromuscular Disorders, Vol. 27: S110-S110
| Item Type: | Journal article |
|---|---|
| Faculties: | Medicine |
| Subjects: | 600 Technology > 610 Medicine and health |
| ISSN: | 0960-8966 |
| Language: | English |
| Item ID: | 52688 |
| Date Deposited: | 14. Jun 2018, 09:50 |
| Last Modified: | 04. Nov 2020, 13:31 |
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