Condition: PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT
rs373674344
in
MCM3AP
gene and
PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT
PMID 29982295
2018 A novel MCM3AP mutation in a Lebanese family with recessive Charcot-Marie-Tooth neuropathy.
PMID 28633435
2017 MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability.
PMID 28969388
2017 Biallelic MCM3AP mutations cause Charcot-Marie-Tooth neuropathy with variable clinical presentation.
PMID 24123876
2013 Identification of pathogenic gene variants in small families with intellectually disabled siblings by exome sequencing.
rs779630101
in
MCM3AP-AS1;MCM3AP
gene and
PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT
PMID 29982295
2018 A novel MCM3AP mutation in a Lebanese family with recessive Charcot-Marie-Tooth neuropathy.
PMID 28969388
2017 Biallelic MCM3AP mutations cause Charcot-Marie-Tooth neuropathy with variable clinical presentation.
PMID 28633435
2017 MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability.
PMID 24123876
2013 Identification of pathogenic gene variants in small families with intellectually disabled siblings by exome sequencing.