[HTML][HTML] Interrogation of Carboxy-Terminus Localized GJA1 Variants Associated with Erythrokeratodermia Variabilis et Progressiva
Although inherited GJA1 (encoding Cx43) gene mutations most often lead to
oculodentodigital dysplasia and related disorders, four variants have been linked to …
oculodentodigital dysplasia and related disorders, four variants have been linked to …
Interrogation of carboxy-terminus localized GJA1 variants associated with erythrokeratodermia variabilis et progressiva
SA Lucaciu, Q Shao, R Figliuzzi, K Barr, D Bai… - International Journal of …, 2022 - ir.lib.uwo.ca
Although inherited GJA1 (encoding Cx43) gene mutations most often lead to oculodentodig-
ital dysplasia and related disorders, four variants have been linked to erythrokeratodermia …
ital dysplasia and related disorders, four variants have been linked to erythrokeratodermia …
Interrogation of Carboxy-Terminus Localized GJA1 Variants Associated with Erythrokeratodermia Variabilis et Progressiva
SA Lucaciu, Q Shao, R Figliuzzi, K Barr, D Bai… - agris.fao.org
Although inherited GJA1 (encoding Cx43) gene mutations most often lead to
oculodentodigital dysplasia and related disorders, four variants have been linked to …
oculodentodigital dysplasia and related disorders, four variants have been linked to …
Interrogation of Carboxy-Terminus Localized GJA1 Variants Associated with Erythrokeratodermia Variabilis et Progressiva
SA Lucaciu, Q Shao, R Figliuzzi… - International …, 2022 - pubmed.ncbi.nlm.nih.gov
Although inherited GJA1 (encoding Cx43) gene mutations most often lead to
oculodentodigital dysplasia and related disorders, four variants have been linked to …
oculodentodigital dysplasia and related disorders, four variants have been linked to …
Interrogation of Carboxy-Terminus Localized GJA1 Variants Associated with Erythrokeratodermia Variabilis et Progressiva.
SA Lucaciu, Q Shao, R Figliuzzi… - International …, 2022 - search.ebscohost.com
Although inherited GJA1 (encoding Cx43) gene mutations most often lead to
oculodentodigital dysplasia and related disorders, four variants have been linked to …
oculodentodigital dysplasia and related disorders, four variants have been linked to …
Interrogation of Carboxy-Terminus Localized GJA1 Variants Associated with Erythrokeratodermia Variabilis et Progressiva
SA Lucaciu, Q Shao, R Figliuzzi, K Barr… - International …, 2022 - search.proquest.com
Although inherited GJA1 (encoding Cx43) gene mutations most often lead to
oculodentodigital dysplasia and related disorders, four variants have been linked to …
oculodentodigital dysplasia and related disorders, four variants have been linked to …
[HTML][HTML] Interrogation of Carboxy-Terminus Localized GJA1 Variants Associated with Erythrokeratodermia Variabilis et Progressiva
SA Lucaciu, Q Shao, R Figliuzzi, K Barr… - … Journal of Molecular …, 2022 - ncbi.nlm.nih.gov
Although inherited GJA1 (encoding Cx43) gene mutations most often lead to
oculodentodigital dysplasia and related disorders, four variants have been linked to …
oculodentodigital dysplasia and related disorders, four variants have been linked to …
[PDF][PDF] Interrogation of Carboxy Terminus Localized GJA1 Variants Associated with Erythrokeratodermia Variabilis et Progressiva
SA Lucaciu, Q Shao, R Figliuzzi, K Barr, D Bai… - Int. J. Mol …, 2022 - researchgate.net
Although inherited GJA1 (encoding Cx43) gene mutations most often lead to
oculodentodigital dysplasia and related disorders, four variants have been linked to …
oculodentodigital dysplasia and related disorders, four variants have been linked to …
Interrogation of Carboxy-Terminus Localized GJA1 Variants Associated with Erythrokeratodermia Variabilis et Progressiva.
SA Lucaciu, Q Shao, R Figliuzzi, K Barr… - … Journal of Molecular …, 2022 - europepmc.org
Although inherited GJA1 (encoding Cx43) gene mutations most often lead to
oculodentodigital dysplasia and related disorders, four variants have been linked to …
oculodentodigital dysplasia and related disorders, four variants have been linked to …
Interrogation of Carboxy-Terminus Localized GJA1 Variants Associated with Erythrokeratodermia Variabilis et Progressiva.
SA Lucaciu, Q Shao, R Figliuzzi, K Barr… - … Journal of Molecular …, 2022 - europepmc.org
Although inherited GJA1 (encoding Cx43) gene mutations most often lead to
oculodentodigital dysplasia and related disorders, four variants have been linked to …
oculodentodigital dysplasia and related disorders, four variants have been linked to …