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Author/Creator Fink, John K.

1. Early‐Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST. Issue 12 (14th September 2022)

Authors:
Mo, Alisa; Saffari, Afshin; Kellner, Melanie; Döbler‐Neumann, Marion; Jordan, Catherine; Srivastava, Siddharth; Zhang, Bo; Sahin, Mustafa; Fink, John K.; Smith, Linsley; Posey, Jennifer E.; Alter, Katharine E.; Toro, Camilo; Blackstone, Craig; Soldatos, Ariane G.; Christie, Michelle; Schüle, Rebe...
Journal:
Movement disorders
Issue:
Volume 37:Issue 12(2022)
Page Start:
2440
Record Type:
Journal Article
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2. Further studies toward a mouse model for biochemical assessment of neuropathic potential of organophosphorus compounds. Issue 12 (7th January 2014)

Authors:
Makhaeva, Galina F.; Rudakova, Elena V.; Hein, Nichole D.; Serebryakova, Olga G.; Kovaleva, Nadezhda V.; Boltneva, Natalia P.; Fink, John K.; Richardson, Rudy J.
Journal:
Journal of applied toxicology
Issue:
Volume 34:Issue 12(2014)
Page Start:
1426
Record Type:
Journal Article
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4. Hereditary Spastic Paraplegia Type 43 (SPG43) is Caused by Mutation in C19orf12. Issue 10 (12th August 2013)

Authors:
Landouré, Guida; Zhu, Peng‐Peng; Lourenço, Charles M.; Johnson, Janel O.; Toro, Camilo; Bricceno, Katherine V.; Rinaldi, Carlo; Meilleur, Katherine G.; Sangaré, Modibo; Diallo, Oumarou; Pierson, Tyler M.; Ishiura, Hiroyuki; Tsuji, Shoji; Hein, Nichole; Fink, John K.; Stoll, Marion; Nicholson, Gar...
Journal:
Human mutation
Issue:
Volume 34:Issue 10(2013:Oct.)
Page Start:
1357
Record Type:
Journal Article
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