Matches in Nanopublications for { ?s ?p "[Here, we identify missense mutations in the calcium channel gene CACNA1H (T-type Ca(V)3.2) in 6 of 461 individuals with ASD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 4 of
4
with 100 items per page.
- NP374825.RAkA93ScUk_KZO9w5eJjdnbqP-eixjOxJMFco7oVoKYA8130_assertion description "[Here, we identify missense mutations in the calcium channel gene CACNA1H (T-type Ca(V)3.2) in 6 of 461 individuals with ASD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374825.RAkA93ScUk_KZO9w5eJjdnbqP-eixjOxJMFco7oVoKYA8130_provenance.
- NP827394.RAsC7thsojDlfKssz2s7bgWjy8GgNM42DgTIyAELSrfBk130_assertion description "[Here, we identify missense mutations in the calcium channel gene CACNA1H (T-type Ca(V)3.2) in 6 of 461 individuals with ASD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP827394.RAsC7thsojDlfKssz2s7bgWjy8GgNM42DgTIyAELSrfBk130_provenance.
- NP811020.RArvo8-iSKjIHaB5CDg8MKrz66mGFlpxL-KOSojSH9iZw130_assertion description "[Here, we identify missense mutations in the calcium channel gene CACNA1H (T-type Ca(V)3.2) in 6 of 461 individuals with ASD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP811020.RArvo8-iSKjIHaB5CDg8MKrz66mGFlpxL-KOSojSH9iZw130_provenance.
- NP553186.RA1YsLvdyjs7Z4z0ty5sX3xTOe17c9OEdu3__j4BMx-yc130_assertion description "[Here, we identify missense mutations in the calcium channel gene CACNA1H (T-type Ca(V)3.2) in 6 of 461 individuals with ASD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP553186.RA1YsLvdyjs7Z4z0ty5sX3xTOe17c9OEdu3__j4BMx-yc130_provenance.