Lv4
543 积分 2022-05-07 加入
Genetics of frontotemporal dementia in China
2天前
已完结
Review for "High prevalence of Bardet-Biedl syndrome in La Réunion Island is due to a founder variant in ARL6/BBS3"
1个月前
已完结
Alu Retrotransposition Event in SPAST Gene as a Novel Cause of Hereditary Spastic Paraplegia
2个月前
已完结
Alu Retrotransposition Event in SPAST Gene as a Novel Cause of Hereditary Spastic Paraplegia
2个月前
已完结
The First Case of Autosomal Recessive Cerebellar Ataxia with Prominent Paroxysmal Non‐kinesigenic Dyskinesia Caused by a Truncating FGF14 Variant in a Turkish Patient
2个月前
已完结
GGC Repeat Expansion of RILPL1 is Associated with Oculopharyngodistal Myopathy
2个月前
已完结
CGG repeat expansion in LOC642361/NUTM2B-AS1 typically presents as oculopharyngodistal myopathy
3个月前
已完结
The clinical, imaging, pathological and genetic landscape of bottom-of-sulcus dysplasia
3个月前
已完结
Rapid Immunodot AQP4 Assay for Neuromyelitis Optica Spectrum Disorder
4个月前
已完结
Multidisciplinary care for rare neurological diseases in China
4个月前
已完结
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