Primary optic atrophy--as a part of the spectrum of other hereditary neurological disorders.

Nair, K R; Safarulla, K

Nair, K R; Safarulla, K.

Article in English | IMSEAR | ID: sea-87156

Subject(s)

Adolescent; Adult; Anophthalmos/genetics; Child; Deafness/genetics; Female; Humans; Male; Middle Aged; Nervous System Diseases/genetics; Optic Atrophy/genetics

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Female / Humans / Male / Child / Optic Atrophy / Anophthalmos / Adolescent / Adult / Deafness / Middle Aged Language: English Year: 1976 Type: Article

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