Matches in Nanopublications for { ?s ?p "[Mutations in the connexin 26 (Cx26) or gap junction beta 2 gene are the leading cause of hereditary nonsyndromic sensorineural hearing loss in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP280989.RAkppUmaH2xHyTlArG62agfTIBskSiIooGbUxp5uClvck130_assertion description "[Mutations in the connexin 26 (Cx26) or gap junction beta 2 gene are the leading cause of hereditary nonsyndromic sensorineural hearing loss in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280989.RAkppUmaH2xHyTlArG62agfTIBskSiIooGbUxp5uClvck130_provenance.
- NP259325.RAxzoN7idgGaXi6lK55qpn3X-zmM4nYZvLMVCXNnwyRto130_assertion description "[Mutations in the connexin 26 (Cx26) or gap junction beta 2 gene are the leading cause of hereditary nonsyndromic sensorineural hearing loss in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP259325.RAxzoN7idgGaXi6lK55qpn3X-zmM4nYZvLMVCXNnwyRto130_provenance.
- NP438351.RAWmdaasF_YJ_2DzzKxsr4LY3jipcchqbqIam1RThTX0I130_assertion description "[Mutations in the connexin 26 (Cx26) or gap junction beta 2 gene are the leading cause of hereditary nonsyndromic sensorineural hearing loss in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP438351.RAWmdaasF_YJ_2DzzKxsr4LY3jipcchqbqIam1RThTX0I130_provenance.
- NP841952.RAuj1ZarbvXEax6ISUUGVa19eQqMeOMfsIMineCw4C9HQ130_assertion description "[Mutations in the connexin 26 (Cx26) or gap junction beta 2 gene are the leading cause of hereditary nonsyndromic sensorineural hearing loss in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP841952.RAuj1ZarbvXEax6ISUUGVa19eQqMeOMfsIMineCw4C9HQ130_provenance.
- NP587683.RAyn7EFJkC8vZb7Wzow-JKycVu0R_LFB9ZjR9n3xpAlIM130_assertion description "[Mutations in the connexin 26 (Cx26) or gap junction beta 2 gene are the leading cause of hereditary nonsyndromic sensorineural hearing loss in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587683.RAyn7EFJkC8vZb7Wzow-JKycVu0R_LFB9ZjR9n3xpAlIM130_provenance.
- NP438349.RAIaFwopfCR0rQXs3LLV9LjYnOwVn56MYK-V9OlJCePI0130_assertion description "[Mutations in the connexin 26 (Cx26) or gap junction beta 2 gene are the leading cause of hereditary nonsyndromic sensorineural hearing loss in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP438349.RAIaFwopfCR0rQXs3LLV9LjYnOwVn56MYK-V9OlJCePI0130_provenance.