Penelope L. Friedman

Internal Medicine
11408 Cedar Ridge Dr
Potomac, MD 20854

Last Updated: 09/26/2026

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Found 3 publications

Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome.

Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome.

Journal: Clinical genetics
Published: July 20, 2016

Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss.

Molecular genetics of MARVELD2 and clinical phenotype in Pakistani and Slovak families segregating DFNB49 hearing loss.

Journal: Human genetics
Published: January 02, 2015

Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86.

Mutations in TBC1D24, a gene associated with epilepsy, also cause nonsyndromic deafness DFNB86.

Journal: American journal of human genetics
Published: October 31, 2013
Showing 1-3 of 3

Last Updated: 09/26/2026