Welcoming articles on genotype-dependent clinical features and diagnostics

[1]  A. Başak,et al.  Cerebellar cognitive-affective syndrome preceding ataxia associated with complex extrapyramidal features in a Turkish SCA48 family , 2019, neurogenetics.

[2]  A. Koch,et al.  Nervous NDRGs: the N-myc downstream–regulated gene family in the central and peripheral nervous system , 2019, neurogenetics.

[3]  W. Chung,et al.  A pathogenic CtBP1 missense mutation causes altered cofactor binding and transcriptional activity , 2019, neurogenetics.

[4]  G. Coppola,et al.  Primary familial brain calcification caused by a novel homozygous MYORG mutation in a consanguineous Italian family , 2019, neurogenetics.

[5]  J. Pilch,et al.  Next-generation sequencing study reveals the broader variant spectrum of hereditary spastic paraplegia and related phenotypes , 2019, neurogenetics.

[6]  A. Tessa,et al.  Clinical and molecular studies in two new cases of ARSACS , 2019, neurogenetics.

[7]  Y. Kishita,et al.  Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndrome , 2019, neurogenetics.

[8]  Q. Waisfisz,et al.  Periodontal Ehlers–Danlos syndrome is associated with leukoencephalopathy , 2018, neurogenetics.

[9]  L. Ptáček,et al.  Episodic disorders: channelopathies and beyond. , 2015, Annual review of physiology.

[10]  J. Mertens,et al.  Excitation-induced ataxin-3 aggregation in neurons from patients with Machado–Joseph disease , 2011, Nature.

[11]  B. Strasser.  Perspectives: molecular medicine. "Sickle cell anemia, a molecular disease". , 1999, Science.

[12]  L. Pauling,et al.  Sickle cell anemia a molecular disease. , 1949, Science.