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Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment
by
Kaheel, Hazem
,
Breß, Andreas
,
Hassan, Mohamed A
,
Shah, Aftab Ali
,
Amin, Mutaz
,
Bakhit, Yousuf H Y
,
Kniper, Marlies
Published in
BMC ear, nose and throat disorders
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Frequency of c.35delG Mutation in GJB2 Gene (Connexin 26) in Syrian Patients with Nonsyndromic Hearing Impairment
by
Kaheel, Hazem
,
Breß, Andreas
,
Hassan, Mohamed A.
,
Shah, Aftab Ali
,
Amin, Mutaz
,
Bakhit, Yousuf H. Y.
,
Kniper, Marlies
Published in
Genetics Research International
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Bmc Ear, Nose And Throat Disorders
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Genetics Research International
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Deafness
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Deoxyribonucleic Acid
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Dna
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Connexin 26
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