Publication | Open Access
Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome
148
Citations
22
References
2001
Year
Mendelian DisorderGenetic DisorderNovel MutationsPathologyMedicineSmith-magenis SyndromeProfound DeafnessMolecular MedicineHearing Loss
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