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» Articles » PMID: 28133733

Additional De Novo Missense Genetic Variants in NALCN Associated with CLIFAHDD Syndrome

Overview
Journal Clin Genet
Specialty Genetics
Date 2017 Jan 31
PMID 28133733
Citations 8
Authors
M Vivero
M T Cho
A Begtrup
I M Wentzensen
L Walsh
K Payne
Y A Zarate
K Bosanko
G B Schaefer
S DeBrosse
L Pollack
K Mason
K Retterer
S DeWard
J Juusola
W K Chung
Affiliations
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