Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene
Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene is a paper indexed in PICO Portal from OpenAlex.
How many citations does Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene have?
Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene has 21 citations in the OpenAlex counts PICO Portal stores.
When was Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene published?
Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene has 2019 year in the PICO Portal index.
What is the open-access status of Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene?
Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene has closed oa status in the PICO Portal index.
What is the DOI of Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene?
The DOI for Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene is on the source record.
What is the PMID of Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene?
The PMID for Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene is on the source record.
What is the OpenAlex record for Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene?
The OpenAlex for Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene is on the source record.