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1 Ergebnisse
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Truncating ARL6IP1 variant as the genetic cause of fatal co..:
Salma M. Wakil
;
Safa Alhissi
;
Haya Al Dossari
...
http://link.springer.com/article/10.1186/s12881-019-0851-6. , 2019
Link:
https://doi.org/10.1186/s12881-019-0851-6
RT Journal T1
Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia
UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:71bceb16ca6a4a7f80e01f6087f9cb35&Exemplar=1&LAN=DE A1 Salma M. Wakil A1 Safa Alhissi A1 Haya Al Dossari A1 Ayesha Alqahtani A1 Sherin Shibin A1 Brahim T. Melaiki A1 Josef Finsterer A1 Amal Al-Hashem A1 Saeed Bohlega A1 Anas M. Alazami PB BMC YR 2019 K1 Hereditary spastic paraplegia K1 Autosomal recessive K1 Whole exome sequencing K1 ADP ribosylation factor like GTPase 6 interacting protein 1 K1 Internal medicine K1 RC31-1245 K1 Genetics K1 QH426-470 JF http://link.springer.com/article/10.1186/s12881-019-0851-6 LK http://dx.doi.org/https://doi.org/10.1186/s12881-019-0851-6 DO https://doi.org/10.1186/s12881-019-0851-6 SF ELIB - SuUB Bremen
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